RESUMEN
Deletions and pathogenic sequence variants in Myeloid Ecotropic Insertion Site 2 (MEIS2) gene have been reported to cause a recognizable triad of intellectual disability, congenital heart malformations, and palatal defects. To date, 18 individuals with de novo pathogenic sequence variants in MEIS2 have been reported in the literature, most with all three cardinal features. We recently saw a young boy, almost 3 years of age, who was known to have mosaic XYY syndrome (47,XYY [23]/46,XY[7]). He presented with atrial and ventricular septal defects, developmental delay, facial dysmorphism, gastroesophageal reflux, undescended testicle, a buried penis with penoscrotal transposition, primary neutropenia, and a branchial cleft sinus. Whole-exome sequencing identified a previously reported in-frame pathogenic deletion (c.998_1000delGAA; p.R333del; NM_170674.4) in MEIS2. His unaffected father was confirmed to have low-level mosaicism for the same MEIS2 variant. The proband represents the 19th reported individual with a pathogenic sequence variant in MEIS2 and expands the phenotypic spectrum to include primary neutropenia, branchial anomalies, and complex genital anomalies. Furthermore, to our knowledge this is the first reported case of mosaicism for a variant in this gene in an apparently unaffected parent. This finding would have implications for recurrence risk counseling for families.
Asunto(s)
Cardiopatías Congénitas/diagnóstico , Proteínas de Homeodominio/genética , Discapacidad Intelectual/diagnóstico , Trastornos de los Cromosomas Sexuales/genética , Factores de Transcripción/genética , Cariotipo XYY/genética , Niño , Predisposición Genética a la Enfermedad , Cardiopatías Congénitas/complicaciones , Cardiopatías Congénitas/genética , Cardiopatías Congénitas/patología , Humanos , Discapacidad Intelectual/complicaciones , Discapacidad Intelectual/genética , Discapacidad Intelectual/patología , Masculino , Mosaicismo , Mutación/genética , Trastornos de los Cromosomas Sexuales/diagnóstico , Trastornos de los Cromosomas Sexuales/patología , Secuenciación del Exoma , Cariotipo XYY/diagnóstico , Cariotipo XYY/patologíaRESUMEN
Sex chromosome abnormalities (SCAs) are characterized by gain or loss of entire sex chromosomes or parts of sex chromosomes with the best-known syndromes being Turner syndrome, Klinefelter syndrome, 47,XXX syndrome, and 47,XYY syndrome. Since these syndromes were first described more than 60 years ago, several papers have reported on diseases and health related problems, neurocognitive deficits, and social challenges among affected persons. However, the generally increased comorbidity burden with specific comorbidity patterns within and across syndromes as well as early death of affected persons was not recognized until the last couple of decades, where population-based epidemiological studies were undertaken. Moreover, these epidemiological studies provided knowledge of an association between SCAs and a negatively reduced socioeconomic status in terms of education, income, retirement, cohabitation with a partner and parenthood. This review is on the aspects of epidemiology in Turner, Klinefelter, 47,XXX and 47,XYY syndrome.
Asunto(s)
Síndrome de Klinefelter/epidemiología , Aberraciones Cromosómicas Sexuales , Cromosomas Sexuales/genética , Síndrome de Turner/epidemiología , Cromosomas Humanos X/genética , Femenino , Humanos , Cariotipificación , Síndrome de Klinefelter/genética , Síndrome de Klinefelter/patología , Masculino , Trastornos de los Cromosomas Sexuales/genética , Trastornos de los Cromosomas Sexuales/patología , Trisomía/genética , Trisomía/patología , Síndrome de Turner/genética , Síndrome de Turner/patología , Cariotipo XYY/genética , Cariotipo XYY/patologíaRESUMEN
An additional Y chromosome occurs in ~1 in 1,000 males, resulting in the karyotype 47,XYY. The phenotype includes tall stature, hypotonia, neuropsychiatric comorbidities, and an increased risk of infertility in adulthood. Little is known about testicular function in childhood and adolescence in 47,XYY. This cross-sectional study aimed to assess testicular function serum biomarkers, including total testosterone, inhibin B, and anti-mullerian hormone (AMH), in 82 boys with XYY (11.3 ± 3.8 years) compared with 66 male controls (11.6 ± 3.8 years). The association of testicular hormones with physical features, neuropsychological phenotype, and magnetoencephalography (MEG) was assessed with multiple linear regression models. Results indicate males with XYY have significantly lower inhibin B (median 84 pg/ml vs. 109 pg/ml, p = .004) and higher AMH (median 41 ng/ml vs. 29 ng/ml, p = .011); however, testosterone, testicular volume, and stretched penile length were not different from controls. In the exploratory analysis of relationships between hormone concentrations and phenotypic assessments, higher inhibin B concentrations were positively correlated with lower BMI and better cognitive, academic, and behavioral outcomes in the XYY group. Testosterone concentrations were positively associated with better behavioral outcomes in boys with XYY. Higher testosterone and inhibin B concentrations were also associated with shorter auditory latencies measured using magnetoencephalography (MEG) in XYY. With a few exceptions, testicular hormones were not associated with phenotypic outcomes in controls. In conclusion, there is evidence of subtle impaired testicular function in boys with XYY and a newly described relationship between measures of testicular function and some aspects of the XYY phenotype.
Asunto(s)
Hormona Antimülleriana/sangre , Inhibinas/sangre , Trastornos de los Cromosomas Sexuales/sangre , Testosterona/sangre , Cariotipo XYY/sangre , Adulto , Encéfalo/diagnóstico por imagen , Encéfalo/patología , Niño , Estudios Transversales , Humanos , Magnetoencefalografía , Masculino , Fenotipo , Trastornos de los Cromosomas Sexuales/diagnóstico por imagen , Trastornos de los Cromosomas Sexuales/genética , Trastornos de los Cromosomas Sexuales/patología , Cariotipo XYY/diagnóstico por imagen , Cariotipo XYY/genética , Cariotipo XYY/patologíaRESUMEN
Infertility is one of the most important and burning issues in present times, as a marked increase in the frequency of infertile cases has been observed all over the world. Chromosomal aneuploidy is among the known factors associated with infertility, and among sex chromosome aneuploidies, 47,XXY and 47,XYY constitute the most common class of chromosome abnormality in human live births. Considerable attention has been given to the somatic abnormalities associated with these conditions, but less is known about their meiotic progression; that is, how sex chromosome imbalance influences the meiotic process. It has been documented that men with the same underlying genetic cause of infertility do not present with uniform pathology, so it is informative to find out how meiotic progression differs in patients with similar chromosomal aneuploidy having different phenotypes. The importance of studying meiotic progression in patients with sex chromosome abnormalities has increased many fold with the introduction of assisted reproductive technologies that have made it possible for infertile men to become biological parents. Hence, exploring the possible consequences of sex chromosome aneuploidy for meiotic chromosome segregation is worthwhile. The objective of this review, in the context of current knowledge, is to discuss problems associated with fertility and progression of meiosis in two relatively common sex chromosome aneuploidies, 47,XXY and 47,XYY, reported in humans.
Asunto(s)
Infertilidad Masculina/genética , Síndrome de Klinefelter/genética , Meiosis/genética , Trastornos de los Cromosomas Sexuales/genética , Cariotipo XYY/genética , Humanos , Infertilidad Masculina/patología , Síndrome de Klinefelter/patología , Masculino , Trastornos de los Cromosomas Sexuales/patología , Cromosomas Sexuales/genética , Espermatogénesis/genética , Espermatozoides/metabolismo , Espermatozoides/patología , Cariotipo XYY/patologíaRESUMEN
Sex chromosome trisomies (SCTs) (XXX, XXY, and XYY karyotypes) are associated with an elevated risk of neurodevelopmental disorders. The range of severity of the phenotype is substantial. We considered whether this variable outcome was related to the presence of copy number variants (CNVs)-stretches of duplicated or deleted DNA. A sample of 125 children with an SCT were compared with 181 children of normal karyotype who had been given the same assessments. First, we compared the groups on measures of overall CNV burden: number of CNVs, total span of CNVs, and likely functional impact (probability of loss-of-function intolerance, pLI, summed over CNVs). Differences between groups were small relative to within-group variance and not statistically significant on overall test. Next, we considered whether a measure of general neurodevelopmental impairment was predicted by pLI summed score, SCT versus comparison group, or the interaction between them. There was a substantial effect of SCT/comparison status but the pLI score was not predictive of outcomes in either group. We conclude that variable presence of CNVs is not a likely explanation for the wide phenotypic variation in children with SCTs. We discuss methodological challenges of testing whether CNVs are implicated in causing neurodevelopmental problems.
Asunto(s)
Variaciones en el Número de Copia de ADN/genética , Trastornos del Neurodesarrollo/genética , Cromosomas Sexuales/genética , Trisomía/genética , Preescolar , Femenino , Humanos , Síndrome de Klinefelter/genética , Síndrome de Klinefelter/patología , Mutación con Pérdida de Función/genética , Masculino , Trastornos del Neurodesarrollo/patología , Fenotipo , Cromosomas Sexuales/patología , Trisomía/patología , Cariotipo XYY/genética , Cariotipo XYY/patologíaRESUMEN
Klinefelter syndrome (KS) is the most frequent sex chromosomal aneuploidy. The karyotype 47,XXY originates from either paternal or maternal meiotic nondisjunction during gametogenesis. KS males are very likely to exhibit marked gonadal dysfunctions, presenting both in severely attenuated spermatogenesis as well as hypergonadotropic hypogonadism. In addition, neurocognitive and psychosocial impairments, as well as cardiovascular, metabolic and bone disorders are often found in KS and might explain for an increased morbidity/mortality. All conditions in KS are likely to be induced by both gene overdosage effects resulting from supernumerary X-chromosomal genes as well as testosterone deficiency. Notwithstanding, the clinical features are highly variable between KS men. Symptoms can become obvious at infancy, childhood, or adolescence. However, the majority of KS subjects is diagnosed during adulthood. KS adolescents require specific attention regarding pubertal development, in order to exploit their remaining fertility potential and allow for timely and tailored testosterone replacement. The chances for sperm retrieval might decline with age and could be hampered by testosterone replacement; therefore, cryostorage of spermatozoa is an option during adolescence, before the decompensation of endocrine and exocrine testicular functions becomes more overt. Sperm from semen or surgically retrieved, in combination with intracytoplasmic sperm injection enables KS males to become biological fathers of healthy children. The aim of this article is to present the current knowledge on KS, to guide clinical care and to highlight research needs.
Asunto(s)
Cromosomas Humanos X/genética , Trastornos Gonadales/terapia , Síndrome de Klinefelter/genética , Trastornos de los Cromosomas Sexuales/terapia , Adolescente , Adulto , Niño , Preescolar , Trastornos Gonadales/genética , Trastornos Gonadales/patología , Gónadas/crecimiento & desarrollo , Gónadas/patología , Humanos , Síndrome de Klinefelter/patología , Masculino , Trastornos de los Cromosomas Sexuales/genética , Trastornos de los Cromosomas Sexuales/patología , Cariotipo XYY/genética , Cariotipo XYY/patología , Adulto JovenRESUMEN
BACKGROUND: 47,XYY is a chromosomal abnormality syndrome that is typically observed in patients with a male phenotype. Few patients with XYY syndrome will have infertility. We here report a case of 46,XY/47,XYY syndrome diagnosed in a patient with a female phenotype. CASE PRESENTATION: A 15-year-old patient with a female phenotype visited our hospital owing to a chief complaint of short stature as of the age of 6 years. She was diagnosed with dwarf syndrome at the age of 10, but no change was noted after 2 months of growth hormone treatment. The patient's height was 136 cm and the weight was 29 kg, both of which were below the third percentile for her age/gender. In addition to short stature, the 4th and 5th metacarpals were short and there was no significant sex development. Karyotype analysis showed 47,XYY, and chromosomal microarray examination showed a chimera of 46,XY/47,XYY. CONCLUSION: This is an extremely rare case of 47,XYY abnormality in a patient with a female phenotype, with only one such known case reported previously. Since the cause is unknown, and symptoms of this syndrome are highly atypical and variable in childhood, clinicians should be aware of this possibility to avoid misdiagnosis and offer counseling and hormone therapy as needed to patients and their parents to improve their quality of life.
Asunto(s)
Trastornos del Crecimiento/patología , Calidad de Vida , Trastornos de los Cromosomas Sexuales/patología , Cariotipo XYY/patología , Adolescente , Femenino , Trastornos del Crecimiento/genética , Humanos , Fenotipo , Pronóstico , Trastornos de los Cromosomas Sexuales/genética , Cariotipo XYY/genéticaAsunto(s)
Aneuploidia , Síndrome de Klinefelter/mortalidad , Trastornos de los Cromosomas Sexuales del Desarrollo Sexual/mortalidad , Trastornos de los Cromosomas Sexuales/mortalidad , Síndrome de la Trisomía 18/mortalidad , Cariotipo XYY/mortalidad , Cromosomas Humanos X/química , Cromosomas Humanos X/genética , Cromosomas Humanos Y/química , Conducto Arterioso Permeable/genética , Conducto Arterioso Permeable/mortalidad , Conducto Arterioso Permeable/patología , Femenino , Cardiopatías Congénitas/genética , Cardiopatías Congénitas/mortalidad , Cardiopatías Congénitas/patología , Defectos del Tabique Interatrial/genética , Defectos del Tabique Interatrial/mortalidad , Defectos del Tabique Interatrial/patología , Defectos del Tabique Interventricular/genética , Defectos del Tabique Interventricular/mortalidad , Defectos del Tabique Interventricular/patología , Humanos , Lactante , Recién Nacido , Cariotipo , Síndrome de Klinefelter/genética , Síndrome de Klinefelter/patología , Masculino , Aberraciones Cromosómicas Sexuales , Trastornos de los Cromosomas Sexuales/genética , Trastornos de los Cromosomas Sexuales/patología , Trastornos de los Cromosomas Sexuales del Desarrollo Sexual/genética , Trastornos de los Cromosomas Sexuales del Desarrollo Sexual/patología , Análisis de Supervivencia , Trisomía/genética , Trisomía/patología , Síndrome de la Trisomía 18/genética , Síndrome de la Trisomía 18/patología , Cariotipo XYY/genética , Cariotipo XYY/patologíaRESUMEN
Objective To explore the feasibility of high-throughput massively parallel genomic DNA sequencing technology for the noninvasive prenatal detection of fetal sex chromosome aneuploidies (SCAs). Methods The study enrolled pregnant women who were prepared to undergo noninvasive prenatal testing (NIPT) in the second trimester. Cell-free fetal DNA (cffDNA) was extracted from the mother's peripheral venous blood and a high-throughput sequencing procedure was undertaken. Patients identified as having pregnancies associated with SCAs were offered prenatal fetal chromosomal karyotyping. Results The study enrolled 10 275 pregnant women who were prepared to undergo NIPT. Of these, 57 pregnant women (0.55%) showed fetal SCA, including 27 with Turner syndrome (45,X), eight with Triple X syndrome (47,XXX), 12 with Klinefelter syndrome (47,XXY) and three with 47,XYY. Thirty-three pregnant women agreed to undergo fetal karyotyping and 18 had results consistent with NIPT, while 15 patients received a normal karyotype result. The overall positive predictive value of NIPT for detecting SCAs was 54.54% (18/33) and for detecting Turner syndrome (45,X) was 29.41% (5/17). Conclusion NIPT can be used to identify fetal SCAs by analysing cffDNA using massively parallel genomic sequencing, although the accuracy needs to be improved particularly for Turner syndrome (45,X).
Asunto(s)
Aneuploidia , ADN/genética , Síndrome de Klinefelter/diagnóstico , Síndrome de Noonan/diagnóstico , Trastornos de los Cromosomas Sexuales del Desarrollo Sexual/diagnóstico , Trastornos de los Cromosomas Sexuales/diagnóstico , Trisomía/diagnóstico , Cariotipo XYY/diagnóstico , Adulto , Cromosomas Humanos X/genética , ADN/sangre , Femenino , Feto , Secuenciación de Nucleótidos de Alto Rendimiento , Humanos , Cariotipificación , Síndrome de Klinefelter/sangre , Síndrome de Klinefelter/genética , Síndrome de Klinefelter/patología , Síndrome de Noonan/sangre , Síndrome de Noonan/genética , Síndrome de Noonan/patología , Valor Predictivo de las Pruebas , Embarazo , Segundo Trimestre del Embarazo , Diagnóstico Prenatal/estadística & datos numéricos , Aberraciones Cromosómicas Sexuales , Trastornos de los Cromosomas Sexuales/sangre , Trastornos de los Cromosomas Sexuales/genética , Trastornos de los Cromosomas Sexuales/patología , Trastornos de los Cromosomas Sexuales del Desarrollo Sexual/sangre , Trastornos de los Cromosomas Sexuales del Desarrollo Sexual/genética , Trastornos de los Cromosomas Sexuales del Desarrollo Sexual/patología , Cromosomas Sexuales/química , Cromosomas Sexuales/patología , Trisomía/genética , Trisomía/patología , Cariotipo XYY/sangre , Cariotipo XYY/genética , Cariotipo XYY/patologíaRESUMEN
The neurocognitive and behavioral profile of individuals with 47,XYY is increasingly documented; however, very little is known about the effect of a supernumerary Y-chromosome on brain development. Establishing the neural phenotype associated with 47,XYY may prove valuable in clarifying the role of Y-chromosome gene dosage effects, a potential factor in several neuropsychiatric disorders that show a prevalence bias toward males, including autism spectrum disorders. Here, we investigated brain structure in 10 young boys with 47,XYY and 10 age-matched healthy controls by combining voxel-based morphometry (VBM) and surface-based morphometry (SBM). The VBM results show the existence of altered gray matter volume (GMV) in the insular and parietal regions of 47,XYY relative to controls, changes that were paralleled by extensive modifications in white matter (WM) bilaterally in the frontal and superior parietal lobes. The SBM analyses corroborated these findings and revealed the presence of abnormal surface area and cortical thinning in regions with abnormal GMV and WMV. Overall, these preliminary results demonstrate a significant impact of a supernumerary Y-chromosome on brain development, provide a neural basis for the motor, speech and behavior regulation difficulties associated with 47,XYY and may relate to sexual dimorphism in these areas.
Asunto(s)
Encéfalo/patología , Trastornos de los Cromosomas Sexuales/patología , Cariotipo XYY/patología , Adolescente , Estudios de Casos y Controles , Niño , Humanos , Imagen por Resonancia Magnética , Masculino , Trastornos de los Cromosomas Sexuales/diagnóstico , Cariotipo XYY/diagnósticoRESUMEN
OBJECTIVE: The 45,X/46,XY and 45,X/47,XYY group of patients includes some of those previously diagnosed with 'mixed gonadal dysgenesis'. Our aim was to establish the clinical and gonadal spectrum, and early surgical management, of patients with chromosomal mosaicism presenting with genital anomalies. PATIENTS AND METHODS: We performed a retrospective review of patients with 45,X/46,XY or 45,X/47,XYY mosaicism presenting with genital ambiguity between 1988 and 2009. At least one gonadal biopsy or gonadectomy specimen was available for each patient. Gonadal histology was re-evaluated by a paediatric pathologist. RESULTS: Of 31 patients with 45,X/46,XY (n = 28) or 45,X/47,XYY (n = 3) mosaicism and genital anomalies, 19 (61%) were raised male. Histology of 46 gonads was available from patients who had undergone a gonadectomy or gonadal biopsy, at a median age of 9.5 months. 18 gonads were palpable at presentation, including 5 (28%) histologically unremarkable testes, 2 streak gonads, and 1 dysgenetic gonad with distinct areas of testicular and ovarian stroma but no oocytes. All intra-abdominal gonads were found to be dysgenetic testes (of which 2 were noted to have pre-malignant changes) or streaks, apart from 1 histologically unremarkable testis. 15 (48%) patients had other anomalies, most commonly cardiac and renal; 4 (13%) had a Turner phenotype. CONCLUSION: The anatomy and gonadal histology of 45,X/46,XY and 45,X/47,XYY individuals with genital ambiguity do not conform to a set pattern, and hence management of each patient should be individualized according to detailed anatomical and histological assessment.
Asunto(s)
Disgenesia Gonadal 46 XY/patología , Disgenesia Gonadal Mixta/genética , Disgenesia Gonadal Mixta/patología , Trastornos de los Cromosomas Sexuales/genética , Trastornos de los Cromosomas Sexuales/patología , Cariotipo XYY/genética , Cariotipo XYY/patología , Preescolar , Bases de Datos Factuales , Trastornos del Desarrollo Sexual/genética , Trastornos del Desarrollo Sexual/patología , Femenino , Disgenesia Gonadal 46 XY/genética , Humanos , Lactante , Recién Nacido , Masculino , Mosaicismo , Fenotipo , Estudios Retrospectivos , Síndrome de Turner/genética , Síndrome de Turner/patologíaRESUMEN
AIM: To assess global and regional brain matter variations associated with XYY syndrome by comparison with Klinefelter syndrome and typical development. METHODS: We used two conceptually distinct voxel-based magnetic resonance imaging methods to examine brain structure in young males with XYY syndrome: (1) volumetric comparison to assess global grey and white matter volumes and (2) support vector machine-based multivariate pattern classification analysis to assess regional neuroanatomy. We assessed verbal, non-verbal, and spatial abilities with the Differential Ability Scales (DAS), and we measured autism diagnostic criteria in eight males with XYY syndrome using the Social Responsiveness Scale and the Autism Diagnostic Interview-Revised (ADI-R). RESULTS: A comparison of 36 typically developing males (mean age 11 y, SD 1 y 9 mo), 31 males with Klinefelter syndrome (mean age 9 y 8 mo, SD 1 y 8 mo), and eight males with XYY syndrome (mean age 11 y 6 mo, SD 1 y 11 mo) showed that total white and grey matter volumes were significantly, or nearly significantly, higher in males with XYY syndrome than in males belonging to the other two groups (grey matter: XYY males vs typically developing males, p<0.006; XYY vs males with Klinefelter syndrome, p<0.001; white matter: XYY males vs typically developing males, p=0.061; XYY males vs males with Klinefelter syndrome, p=0.004). Voxel-based multivariate pattern classification analysis indicates that, after controlling for global volumes, regional brain variations in XYY syndrome are more like those found in Klinefelter syndrome than those occurring in typical development. Further, visualization of classification parameters suggests that insular and frontotemporal grey matter and white matter, including known language areas, are reduced in males with XYY syndrome, similar to what is seen in Klinefelter syndrome. In males with XYY syndrome, DAS verbal and non-verbal scores were significantly lower than in typically developing participants (both p<0.001). DAS scores were not significantly different between XYY and Klinefelter syndrome groups. In five of eight males with XYY syndrome, the Social Responsiveness Scale score exceeded the cut-off for a likely diagnosis of autism spectrum disorder (ASD). In three of eight males with XYY syndrome, the ADI-R score met the cut-off for ASD diagnosis; in another two, ADI-R scores within the social and communication domains met the cut-off values for a diagnosis of ASD. INTERPRETATION: The results suggest that genetic variations associated with XYY syndrome result in increased brain matter volumes, a finding putatively related to the increased frequency of ASDs in individuals with this condition. In addition, frontotemporal grey and white matter reductions in XYY syndrome provide a likely neuroanatomical correlate for observed language impairments.
Asunto(s)
Encéfalo/patología , Cromosomas Humanos X/genética , Cromosomas Humanos Y/genética , Síndrome de Klinefelter/patología , Imagen por Resonancia Magnética/métodos , Trastornos de los Cromosomas Sexuales/patología , Cariotipo XYY/patología , Encéfalo/fisiopatología , Niño , Trastornos Generalizados del Desarrollo Infantil/diagnóstico , Trastornos Generalizados del Desarrollo Infantil/genética , Trastornos Generalizados del Desarrollo Infantil/patología , Trastornos Generalizados del Desarrollo Infantil/fisiopatología , Lóbulo Frontal/patología , Lóbulo Frontal/fisiopatología , Humanos , Síndrome de Klinefelter/genética , Síndrome de Klinefelter/fisiopatología , Imagen por Resonancia Magnética/instrumentación , Masculino , Pruebas Neuropsicológicas , Trastornos de los Cromosomas Sexuales/genética , Trastornos de los Cromosomas Sexuales/fisiopatología , Lóbulo Temporal/patología , Lóbulo Temporal/fisiopatología , Cariotipo XYY/genética , Cariotipo XYY/fisiopatologíaRESUMEN
OBJECTIVE: To evaluate the presence of spermatogonia in men diagnosed with Klinefelter syndrome (KS), in whom no testicular spermatozoa were recovered by testicular sperm extraction. DESIGN: Retrospective case series. SETTING: University hospital. PATIENT(S): Testicular samples from 22 nonmosaic 47,XXY men, aged 24-43 years, with no spermatozoa at multiple biopsies. INTERVENTION(S): Paraffin-embedded testicular tissue was sectioned and stained with hematoxylin-eosin, and immunostainings were performed for both MAGE-A4 and vimentin. MAIN OUTCOME MEASURE(S): The presence of spermatogonia. RESULT(S): Massive fibrosis and hyalinization were observed in all men with KS. Spermatogonia were observed in 4 of 22 men with KS, with differentiation up to the spermatocyte level in 2 of them. CONCLUSION(S): A few men with KS, having no spermatozoa after testicular sperm extraction, still had few spermatogonia. These patients may eventually benefit from in vitro maturation using spermatogonial stem cells. The adult KS population can thus be divided into three subgroups: one subgroup showing focal spermatogenesis, a second having spermatogonia, and a third group in which no germ cells can be recovered. Further research is necessary to unravel the mechanism leading to these different patterns in patients with KS.
Asunto(s)
Síndrome de Klinefelter/genética , Síndrome de Klinefelter/patología , Trastornos de los Cromosomas Sexuales/genética , Trastornos de los Cromosomas Sexuales/patología , Recuperación de la Esperma , Espermatogonias/patología , Espermatozoides/patología , Cariotipo XYY/genética , Cariotipo XYY/patología , Adulto , Antígenos de Neoplasias/análisis , Bélgica , Biomarcadores/análisis , Biopsia , Hospitales Universitarios , Humanos , Inmunohistoquímica , Síndrome de Klinefelter/metabolismo , Masculino , Proteínas de Neoplasias/análisis , Adhesión en Parafina , Estudios Retrospectivos , Trastornos de los Cromosomas Sexuales/metabolismo , Recuento de Espermatozoides , Espermatogénesis/genética , Espermatogonias/química , Espermatozoides/química , Vimentina/análisis , Cariotipo XYY/metabolismo , Adulto JovenRESUMEN
Sex chromosome distribution and aneuploidy as well as germ cell degeneration were evaluated in meiotic and post-meiotic cells from an infertile XYY male. Sex chromosome distribution was assessed by multicolour fluorescence in situ hybridization on meiotic preparations. Post-meiotic cell aneuploidy was characterized by a method combining multicolour fluorescence in situ hybridization and immunocytochemistry using the proacrosin-specific monoclonal antibody (mAb 4D4). TUNEL assay was carried out on seminiferous tubules to evaluate germ cell degeneration. At the prophase stage of the first meiotic division, 63.64% of cells at the pachytene stage carried three sex chromosomes. The ratio of X-bearing to Y-bearing spermatids and spermatozoa differed significantly from 1 : 1 with an excess of Y-bearing spermatids and spermatozoa. The frequency of hyperhaploid XY spermatids was increased in the XYY male, as well as the incidence of YY, XY and disomic 18 ejaculated spermatozoa. A preferential elimination of germ cells by apoptosis occurred in spermatocytes I. The persistence of the extra Y chromosome during meiosis of an XYY male is associated with a high rate of spermatocyte I degeneration and a low rate of aneuploid spermatozoa.
Asunto(s)
Infertilidad Masculina/genética , Infertilidad Masculina/patología , Cariotipo XYY/genética , Cariotipo XYY/patología , Adulto , Aneuploidia , Apoptosis , Fragmentación del ADN , Humanos , Hibridación Fluorescente in Situ , Etiquetado Corte-Fin in Situ , Masculino , Meiosis , Espermátides/fisiología , Espermátides/ultraestructura , Espermatocitos/fisiología , Espermatocitos/ultraestructura , Espermatozoides/fisiologíaRESUMEN
Studies on individuals with sex chromosome anomalies have demonstrated the promoting effect of the Y chromosome on tooth crown enamel and dentin growth. The present research investigated permanent tooth root lengths in 47,XYY males. The measurements were made from panoramic radiographs. The results indicate longer tooth roots in 47,XYY males compared with those in control males and females. The promoting effect of the Y chromosome on dental growth thus continues in the form of root dentin after the completion of crown growth. The results, together with those on tooth crown sizes in 47,XYY males, suggest that growth excesses are evident and final, beginning a few months after birth and continuing up to the age of 14 years, at least. The excess root dentin growth in 47,XYY males, as well as sexual dimorphism in the growth of crown and root dentin, might be caused by the same factor on the Y chromosome.
Asunto(s)
Dentinogénesis/genética , Raíz del Diente/crecimiento & desarrollo , Cariotipo XYY/fisiopatología , Adolescente , Adulto , Estudios de Casos y Controles , Femenino , Humanos , Masculino , Cariotipo XYY/patologíaRESUMEN
XX 'pure' gonadal dysgenesis is a disease related to Turner's syndrome. Patients of this disease are characterized by normal female external genitalia, bilateral streak gonads, amenorrhea and sexual infantilism. Recently, it has been reported that point mutations of the FSH receptor gene may be one of cause of this disease. The relationship between criminal behavior and XYY syndrome is still controversial. Increased incidence of disomic sperm in 47,XYY males has been reported by fluorescent in situ hybridization(FISH). Genetic counseling should be done when they undergo intracytoplasmic sperm injection.
Asunto(s)
Disgenesia Gonadal 46 XX , Cariotipo XYY , Femenino , Fertilidad , Asesoramiento Genético , Disgenesia Gonadal 46 XX/genética , Disgenesia Gonadal 46 XX/patología , Gónadas/patología , Humanos , Hibridación Fluorescente in Situ , Masculino , Mutación Puntual , Receptores de HFE/genética , Inyecciones de Esperma Intracitoplasmáticas , Espermatozoides , Síndrome de Turner , Cariotipo XYY/genética , Cariotipo XYY/patologíaRESUMEN
We report on a 34-year-old developmentally disabled man referred to our clinic for evaluation of possible Prader-Willi syndrome on the basis of obesity and voracious appetite. Cytogenetic and molecular analysis revealed a 47, XYY karyotype and the presence of a trinucleotide repeat expansion resulting in fragile X syndrome. To our knowledge, this is the first report of concurrence of XYY and fragile X syndrome in the medical literature. Review of sex chromosome abnormalities associated with fragile X syndrome and phenotypic considerations are presented.
Asunto(s)
Síndrome del Cromosoma X Frágil/patología , Síndrome de Prader-Willi/patología , Cariotipo XYY/patología , Anomalías Múltiples/genética , Anomalías Múltiples/patología , Adulto , Síndrome del Cromosoma X Frágil/genética , Humanos , Discapacidad Intelectual/patología , Masculino , Obesidad/patología , Fenotipo , Síndrome de Prader-Willi/genética , Cariotipo XYY/genéticaRESUMEN
We describe a boy with XYY male accompanied with essential thrombocythemia. This is, to our knowledge, the first complete case report of the kind in the pediatric literature. The patient was asymptomatic, but at age 5 his platelet count had increased to 145.5 x 10(4)/microL, and he was diagnosed as having essential thrombocythemia based on the diagnostic criteria of the Polycythemia Vera Study Group. At that time, it was discovered by chromosome analysis of both bone marrow and peripheral blood cells that he was XYY male. At times during the clinical course when his platelet count was 94.1 x 10(4)/microL, his serum thrombopoietin (measured by enzyme-linked immunosorbent assay) was 1.09 fmol/mL, which was normal for his age. Aspirin was administered, and he remained asymptomatic throughout the course. After 2 years, he underwent a spontaneous remission. Because of the small number of reported cases, we have been unable to determine the relation between XYY males and essential thrombocythemia.
Asunto(s)
Trombocitosis/genética , Cariotipo XYY/sangre , Aspirina/administración & dosificación , Células Sanguíneas/patología , Células Sanguíneas/ultraestructura , Células de la Médula Ósea/patología , Células de la Médula Ósea/ultraestructura , Preescolar , Supervivencia sin Enfermedad , Humanos , Masculino , Recuento de Plaquetas , Trombocitosis/tratamiento farmacológico , Cariotipo XYY/patologíaRESUMEN
Eight adult, Finnish 47,XYY males were compared with population male and female controls and, in addition, three of them were compared with first-degree male relatives. Linear and angular measurements were made from standardized lateral cephalograms of patients and normal population controls from the "Kvantti" study series. In both comparisons the craniofacial dimensions in 47,XYY males were larger than those in population male and female controls. Their craniofacial proportions and plane angles were similar to those of normal men except for a larger lower facial height with posterior rotation of the mandible and a tendency to bimaxillary protrusion, a longer cranial base and a lesser cranial-base angle. Thus the supernumerary Y chromosomal gene(s) in 47,XYY males may result in larger craniofacial dimensions than in normal males, without substantial effects on dimensional ratios and plane angles. This general metric pattern is similar to that observed in relation to many adult body and head dimensions, and the dental arches and tooth crowns, of 47,XYY males. The foramen magnum in 47,XYY males was smaller in the sagittal plane than that of normal males and females.
Asunto(s)
Cara , Huesos Faciales/patología , Cráneo/patología , Cariotipo XYY/patología , Adolescente , Adulto , Antropometría , Cefalometría , Mentón/patología , Arco Dental/patología , Femenino , Finlandia , Foramen Magno/patología , Humanos , Masculino , Maloclusión/patología , Mandíbula/patología , Maxilar/patología , Persona de Mediana Edad , Odontometría , Rotación , Silla Turca/patología , Base del Cráneo/patología , Corona del Diente/patología , Cariotipo XYY/genética , Cromosoma YRESUMEN
Chromosome analysis was performed on a 3-year-old boy because of bilateral radioulnar synostosis and demonstrated a mosaic karyotype 46,XY/47,XYY/48,XYYY. He had minor facial anomalies and mild intellectual delay. He appears to be the youngest patient reported with this rare chromosome complement. His father, mother, and brother had normal chromosomes. Fluorescence in situ hybridization (FISH) was performed on the propositus and his father with the Y chromosome heterochromatic probe (pHY3.4) to add to the evaluation of mosaicism.