RESUMEN
Two children are presented who have a distinct syndrome of multiple buccolingual frenula, a stiff and short fifth finger with small nails, a hypothalamic hamartoma, mild to moderate neurological impairment, and mild endocrinological symptoms. No variant assessed to be pathogenic or likely pathogenic was detected in the GLI3 gene in either child. This syndrome appears to be distinct from the inherited Pallister-Hall syndrome associated with GLI3 variants, which is characterized by hypothalamic hamartoma, mesoaxial polydactyly, and other anomalies. In the individuals described here, manifestations outside of the central nervous system were milder and the mesoaxial polydactyly, which is common in individuals with Pallister-Hall syndrome, was absent. Instead, these children had multiple buccolingual frenula together with the unusual appearance of the fifth digit. It remains unclear whether these two individuals represent a separate nosologic entity or if they represent a milder manifestation of one of the more severe syndromes associated with a hypothalamic hamartoma.
Asunto(s)
Hamartoma , Enfermedades Hipotalámicas , Síndrome de Pallister-Hall , Polidactilia , Niño , Humanos , Síndrome de Pallister-Hall/diagnóstico , Síndrome de Pallister-Hall/genética , Hamartoma/diagnóstico , Hamartoma/genética , Hamartoma/patología , Enfermedades Hipotalámicas/diagnóstico , Enfermedades Hipotalámicas/genética , Enfermedades Hipotalámicas/patología , Polidactilia/genéticaRESUMEN
OBJECTIVE: To explore the clinical and genetic characteristics of a child with Pallister-Hall syndrome (PHS). METHODS: DNA was extracted from peripheral blood sample from the child and subjected to whole exome sequencing. Suspected variants were verified by Sanger sequencing of his family members. RESULTS: Genetic testing revealed that the child has harbored a heterozygous c.3320_3330delGGTACGAGCAG (p.G1107Afs×18) variant of the GLI3 gene. Neither parent was found to carry the same variant. CONCLUSION: The c.3320_3330delGGTACGAGCAG (p.G1107Afs×18) frameshift variant of the GLI3 gene probably underlay the pathogenesis of PHS in this child. Genetic testing should be considered for patients featuring hypothalamic hamartoma and central polydactyly.
Asunto(s)
Hamartoma , Síndrome de Pallister-Hall , Polidactilia , Humanos , Niño , Síndrome de Pallister-Hall/genética , Factores de Transcripción de Tipo Kruppel/genética , Proteína Gli3 con Dedos de Zinc/genética , Polidactilia/genética , Hamartoma/genética , Hamartoma/patología , Proteínas del Tejido Nervioso/genéticaRESUMEN
Pallister-Hall syndrome (PHS) is a rare autosomal dominant disease diagnosed by the presence of hypothalamic hamartoma, mesoaxial polydactyly and a truncating variant in the middle third of the GLI-Kruppel family member 3 (GLI3) gene. PHS may also include a wide range of clinical phenotypes affecting multiple organ systems including congenital anomalies of the kidney and urinary tract (CAKUT). The observed clinical phenotypes are consistent with the essential role of GLI3, a transcriptional effector in the hedgehog (Hh) signaling pathway, in organogenesis. However, the mechanisms by which truncation of GLI3 in PHS results in such a variety of clinical phenotypes with variable severity, even within the same organ, remain unclear. In this study we focus on presentation of CAKUT in PHS. A systematic analysis of reported PHS patients (n = 78) revealed a prevalence of 26.9% (21/78) of CAKUT. Hypoplasia (± dysplasia) and agenesis were the two main types of CAKUT; bilateral and unilateral CAKUT were reported with equal frequency. Examination of clinical phenotypes with CAKUT revealed a significant association between CAKUT and craniofacial defects, bifid epiglottis and a Disorder of Sex Development, specifically affecting external genitalia. Lastly, we determined that PHS patients with CAKUT predominately had substitution type variants (as opposed to deletion type variants in non-CAKUT PHS patients) in the middle third of the GLI3 gene. These results provide a foundation for future work aimed at uncovering the molecular mechanisms by which variant GLI3 result in the wide range and severity of clinical features observed in PHS.
Asunto(s)
Anomalías Múltiples , Síndrome de Pallister-Hall , Sistema Urinario , Humanos , Síndrome de Pallister-Hall/diagnóstico , Síndrome de Pallister-Hall/genética , Proteína Gli3 con Dedos de Zinc/genética , Factores de Transcripción de Tipo Kruppel/genética , Anomalías Múltiples/genética , Proteínas del Tejido Nervioso/genética , Proteínas Hedgehog , RiñónRESUMEN
BACKGROUND: Pallister-Hall syndrome (OMIM #146510) is a rare autosomal dominant condition caused by a mutation in the GLI3 gene. The cardinal feature of Pallister-Hall syndrome is the presence of hypothalamic hamartomas, which may manifest with seizures, panhypopituitarism and visual impairment. In Pallister-Hall syndrome, dysplastic histogenetic processes responsible for hypothalamic hamartomas are thought to disrupt early craniofacial development. The clinical presentation of Pallister-Hall syndrome may include: characteristic facies (low-set and posteriorly angulated ears, short nose with flat nasal bridge), cleft palate and uvula, bifid epiglottis and laryngotracheal cleft, limb anomalies (e.g., polysyndactyly, short limbs and nail dysplasia), anal atresia, genitourinary abnormalities and congenital heart defects. CASE PRESENTATION: We report the case of two monochorionic diamniotic twins diagnosed with Pallister-Hall syndrome during the neonatal period, after the identification of a hypothalamic hamartoma on day 1 by cerebral ultrasound scan, later confirmed by brain magnetic resonance imaging. Cerebral ultrasound and magnetic resonance imaging presentations were identical in both twins. DISCUSSION AND CONCLUSIONS: We review previously published cases (four reports) of hypothalamic hamartomas identified via cerebral ultrasound and compare reported ultrasonographic features. Main differential diagnoses based on cerebral ultrasound findings are discussed. Full description of typical magnetic resonance imaging appearance is also provided. This is the first case reported in the literature of monochorionic diamniotic twins affected by genetically confirmed Pallister-Hall syndrome with identical hypothalamic hamartomas at cerebral ultrasound and magnetic resonance imaging. Moreover, this paper adds to the existing literature on the sonographic appearance of hypothalamic hamartomas. Considering the consistency in hypothalamic hamartomas' sonographic appearance, we support the use of cerebral ultrasound as a first-line neuroimaging modality in case of clinical suspicion of Pallister-Hall syndrome.
Asunto(s)
Enfermedades Hipotalámicas , Síndrome de Pallister-Hall , Hamartoma , Humanos , Enfermedades Hipotalámicas/complicaciones , Enfermedades Hipotalámicas/diagnóstico por imagen , Recién Nacido , Neuroimagen , Síndrome de Pallister-Hall/complicaciones , Síndrome de Pallister-Hall/diagnóstico por imagen , Síndrome de Pallister-Hall/genética , Gemelos MonocigóticosRESUMEN
Pallister-Hall syndrome, typically caused by germline or de novo variants within the GLI3 gene, has key features of hypothalamic hamartoma and polydactyly. Recently, a few similar cases have been described with bi-allelic SMO variants. We describe two siblings born to non-consanguineous unaffected parents presenting with hypothalamic hamartoma, post-axial polydactyly, microcephaly amongst other developmental anomalies. Previous clinical diagnostic exome analysis had excluded a pathogenic variant in GLI3. We performed exome sequencing re-analysis and identified bi-allelic SMO variants including a missense and synonymous variant in both affected siblings. We functionally characterised this synonymous variant showing it induces exon 8 skipping within the SMO transcript. Our results confirm bi-allelic SMO variants as an uncommon cause of Pallister-Hall syndrome and describe a novel exon-skipping mechanism, expanding the molecular architecture of this new clinico-molecular disorder.
Asunto(s)
Hamartoma , Enfermedades Hipotalámicas , Síndrome de Pallister-Hall , Polidactilia , Hamartoma/genética , Humanos , Enfermedades Hipotalámicas/diagnóstico , Enfermedades Hipotalámicas/genética , Síndrome de Pallister-Hall/diagnóstico , Síndrome de Pallister-Hall/genética , Polidactilia/genética , Receptor SmoothenedRESUMEN
Variants in transcriptional activator Gli Kruppel Family Member 3 (GLI3) have been reported to be associated with several phenotypes including Greig cephalopolysyndactyly syndrome (MIM #175700), Pallister-Hall syndrome (PHS) (MIM #146510), postaxial polydactyly types A1 (PAPA1) and B (PAPB) (MIM #174200), and preaxial polydactyly type 4 (MIM #174700). All these disorders follow an autosomal dominant pattern of inheritance. Hypothalamic hamartomas (MIM 241800) is associated with somatic variants in GLI3. We report a related couple with parents having PAPA1 and PAPB, who had a fetus with a phenotype most compatible with PHS. Molecular analyses demonstrated homozygosity for a pathogenic GLI3 variant (c.1927C > T; p. Arg643*) in the fetus and heterozygosity in the parents. The genetic analysis in this family demonstrates that heterozygosity and homozygosity for the same GLI3 variant can cause a different phenotype. Furthermore, the occurrence of Pallister-Hall-like syndrome in a homozygous patient should be taken into account in genetic counseling of families with PAPA1/PAPB.
Asunto(s)
Anomalías Múltiples/genética , Dedos/anomalías , Proteínas del Tejido Nervioso/genética , Síndrome de Pallister-Hall/genética , Polidactilia/genética , Dedos del Pie/anomalías , Proteína Gli3 con Dedos de Zinc/genética , Anomalías Múltiples/diagnóstico por imagen , Anomalías Múltiples/patología , Feto Abortado/diagnóstico por imagen , Feto Abortado/patología , Adulto , Femenino , Dedos/diagnóstico por imagen , Dedos/patología , Heterocigoto , Homocigoto , Humanos , Masculino , Síndrome de Pallister-Hall/complicaciones , Síndrome de Pallister-Hall/diagnóstico por imagen , Síndrome de Pallister-Hall/patología , Linaje , Fenotipo , Polidactilia/complicaciones , Polidactilia/diagnóstico por imagen , Polidactilia/patología , Dedos del Pie/diagnóstico por imagen , Dedos del Pie/patologíaRESUMEN
A laryngotracheoesophageal cleft (LC) is a rare congenital anomaly of the upper aerodigestive tract resulting from the absence of fusion of the posterior cricoid lamina, which affects an abnormal communication between the larynx, trachea and esophagus. The genetic etiology of LC remains elusive. The involvement of genetic factors in the development of LC is suggested by reports of familial occurrence, and the increased prevalence of component features among first-degree relatives of affected individuals and murine knockout models. No consistent pattern of inheritance has been found in nonsyndromic patients, except for cases associated with described syndromes. Once the syndrome related to the laryngeal cleft is considered, an active search for the cleft must be initiated. The genetic evaluation of patients with LCs should be guided by the type and location of the malformation, specific medical history and a detailed physical examination. The application of genetic approaches, such as microarrays and exome sequencing might lead to elucidating the etiology of LCs.
Asunto(s)
Canal Anal/anomalías , Artrogriposis/genética , Síndrome CHARGE/genética , Anomalías Congénitas/genética , Anomalías Craneofaciales/genética , Síndrome de DiGeorge/genética , Enfermedades del Oído/genética , Oído/anomalías , Esófago/anomalías , Cardiopatías Congénitas/genética , Hipertelorismo/genética , Hipopituitarismo/genética , Hipospadias/genética , Discapacidad Intelectual/genética , Riñón/anomalías , Laringe/anomalías , Deformidades Congénitas de las Extremidades/genética , Síndrome de Pallister-Hall/genética , Columna Vertebral/anomalías , Tráquea/anomalías , Anomalías Congénitas/diagnóstico , HumanosAsunto(s)
Polidactilia/diagnóstico por imagen , Ultrasonografía Prenatal , Acrocefalosindactilia/complicaciones , Acrocefalosindactilia/diagnóstico , Acrocefalosindactilia/genética , Amniocentesis , Muestra de la Vellosidad Coriónica , Trastornos de la Motilidad Ciliar/complicaciones , Trastornos de la Motilidad Ciliar/diagnóstico , Trastornos de la Motilidad Ciliar/genética , Diagnóstico Diferencial , Encefalocele/complicaciones , Encefalocele/diagnóstico , Encefalocele/genética , Femenino , Pruebas Genéticas , Humanos , Imagenología Tridimensional , Análisis por Micromatrices , Síndrome de Pallister-Hall/complicaciones , Síndrome de Pallister-Hall/diagnóstico , Síndrome de Pallister-Hall/genética , Enfermedades Renales Poliquísticas/complicaciones , Enfermedades Renales Poliquísticas/diagnóstico , Enfermedades Renales Poliquísticas/genética , Polidactilia/etiología , Embarazo , Pronóstico , Retinitis Pigmentosa/complicaciones , Retinitis Pigmentosa/diagnóstico , Retinitis Pigmentosa/genética , Distribución por Sexo , Síndrome de Smith-Lemli-Opitz/diagnóstico , Síndrome de Smith-Lemli-Opitz/genética , Síndrome de la Trisomía 13/complicaciones , Síndrome de la Trisomía 13/diagnóstico , Síndrome de la Trisomía 13/genéticaAsunto(s)
Anomalías Múltiples/diagnóstico , Anomalías Múltiples/genética , Trastornos de los Cromosomas/genética , Síndrome de Pallister-Hall/genética , Adulto , Trastornos de los Cromosomas/diagnóstico , Cromosomas Humanos Par 12/genética , Femenino , Humanos , Recién Nacido , Síndrome de Pallister-Hall/diagnóstico , EmbarazoRESUMEN
INTRODUCTION: Pallister-Hall syndrome (PHS) is a rare autosomal dominant syndrome characterized by polydactyly, bifid or shortened epiglottis, visceral anomalies, hypothalamic hamartoma often combined with hypopituitarism. PHS is characterized by significant variability in the expression of clinical symptoms. The clinical course ranges from mild with a good prognosis to severe and which can lead to death during the neonatal period. CASE REPORT: Two-years-old girl with facial dysmorphia, skeletal malformations of hand and feet and growth hormone deficiency. PHS was diagnosed on the basis of the presented symptoms and genetic tests. SUMMARY: Skeletal malformations, such as polydactyly or oligodactyly, are a markers which can be associated with endocrinological disorders. Quick and correct diagnosis would help in planning treatment during childhood and giving family counseling, including prenatal advice regarding the next pregnancy of the child's mother.
Asunto(s)
Síndrome de Pallister-Hall/diagnóstico , Preescolar , Femenino , Humanos , Síndrome de Pallister-Hall/genética , Síndrome de Pallister-Hall/terapiaRESUMEN
BACKGROUND: A proper balance between the activator and the repressor form of GLI3, a zinc-finger transcription factor downstream of hedgehog signaling, is essential for proper development of various organs during development. Mutations in different domains of the GLI3 gene underlie several congenital diseases including Greig cephalopolysyndactyly syndrome (GCPS) and Pallister-Hall syndrome (PHS). CASE PRESENTATION: Here, we describe the case of an overlapped phenotype of these syndromes with agenesis of the gallbladder and the pancreas, bearing a c.2155 C > T novel likely pathogenic variant of GLI3 gene by missense point mutation causing p.P719S at the proteolytic cleavage site. CONCLUSIONS: Although agenesis of the gallbladder and the pancreas is uncommon in GLI3 morphopathy, a slight difference in the gradient or the balance between activator and repressor in this case may hinder sophisticated spatial and sequential hedgehog signaling that is essential for proper development of gallbladder and pancreas from endodermal buds.
Asunto(s)
Acrocefalosindactilia/genética , Vesícula Biliar/anomalías , Proteínas del Tejido Nervioso/genética , Síndrome de Pallister-Hall/genética , Páncreas/anomalías , Proteína Gli3 con Dedos de Zinc/genética , Anomalías Múltiples/genética , Anomalías Múltiples/patología , Acrocefalosindactilia/patología , Feto , Humanos , Masculino , Mutación Missense , Síndrome de Pallister-Hall/patología , Fenotipo , Mutación PuntualRESUMEN
Pallister Hall syndrome is autosomal dominant disorder usually diagnosed in infants and children. Current diagnostic criteria include presence of hypothalamic hamartoma, post axial polydactyly and positive family history, but the disease has variable manifestations. Herein we report Pallister Hall syndrome diagnosed in a family where both patients were adults. A 59 year old man developed seizures 4 years prior to our evaluation of him, at which time imaging showed a hypothalamic hamartoma. The seizures were controlled medically. He did well until he had visual changes after a traumatic head injury. Repeat MRI showed slight expansion of the mass with formal visual field testing demonstrating bitemporal hemianopsia. There was no evidence of pituitary dysfunction except for large urine volume. He underwent surgery to debulk the hamartoma and the visual field defects improved. There was no hypopituitarism post-operatively, and the polydyspia resolved. His 29 year old daughter also had seizures and hypothalamic hamartoma. Both patients had had polydactyly with prior surgical correction in childhood. The daughter underwent genetic testing, which revealed a previously undescribed heterozygous single base pair deletion in exon 13 of the GLI3 gene causing a frameshift mutation. Further investigation into family history revealed multiple members in previous generations with polydactyly and/or seizures. Pallister-Hall syndrome is caused by an inherited autosomal dominant or de novo mutation in GLI3 gene. This rare syndrome has not had prevalence defined, however. Generally, diagnoses are made in the pediatric population. Our report adds to the few cases detected in adulthood.
Asunto(s)
Mutación del Sistema de Lectura , Proteínas del Tejido Nervioso/genética , Síndrome de Pallister-Hall/diagnóstico , Proteína Gli3 con Dedos de Zinc/genética , Adulto , Análisis Mutacional de ADN , Diagnóstico Tardío , Familia , Femenino , Humanos , Masculino , Persona de Mediana Edad , Síndrome de Pallister-Hall/genéticaRESUMEN
Disruption of normal ciliary function results in a range of diseases collectively referred to as ciliopathies. Here we report a child with a phenotype that overlapped with Joubert, oral-facial-digital, and Pallister-Hall syndromes including brain, limb, and craniofacial anomalies. We performed exome-sequence analysis on a proband and both parents, filtered for putative causative variants, and Sanger-verified variants of interest. Identified variants in CLUAP1 were functionally analyzed in a Xenopus system to determine their effect on ciliary function. Two variants in CLUAP1 were identified through exome-sequence analysis, Chr16:g.3558407T>G, c.338T>G, p.(Met113Arg) and Chr16:g.3570011C>T, c.688C>T, p.(Arg230Ter). These variants were rare in the Exome Aggregation Consortium (ExAC) data set of 65,000 individuals (one and two occurrences, respectively). Transfection of mutant CLUAP1 constructs into Xenopus embryos showed reduced protein levels p.(Arg230Ter) and reduced intraflagellar transport p.(Met113Arg). The genetic data show that these variants are present in an affected child, are rare in the population, and result in reduced, but not absent, intraflagellar transport. We conclude that biallelic mutations in CLUAP1 resulted in this novel ciliopathy syndrome in the proband.
Asunto(s)
Anomalías Múltiples/genética , Antígenos de Neoplasias/genética , Cerebelo/anomalías , Anomalías del Ojo/genética , Enfermedades Renales Quísticas/genética , Síndromes Orofaciodigitales/genética , Retina/anomalías , Adulto , Animales , Antígenos de Neoplasias/metabolismo , Proteínas Portadoras/genética , Niño , Anomalías Craneofaciales/genética , Exoma , Femenino , Flagelos/genética , Heterocigoto , Humanos , Masculino , Síndrome de Pallister-Hall/genética , Fenotipo , Polidactilia/genética , Secuenciación del Exoma , Xenopus/genéticaRESUMEN
Pallister-Hall syndrome was initially recognized under fairly unique circumstances involving exhumation of the very first case. The first two cases had dramatic and unusual features including a hypothalamic hamartoblastoma, imperforate anus, an unusual type of polydactyly with the extra digit being central, hypopituitarism with secondary hypoadrenalism, and lethality after birth (probably due to hypoadrenalism). Within a short time frame, four additional cases were identified. As the full spectrum and variability of anomalies was recognized, it became clear that it was not such a rare disorder. Shortly after familial cases were recognized, the responsible gene was identified at GLI3. However, since other different conditions also involved GLI3, elaborating the domains of the gene and the types of mutations needed to be defined in order to have a clear correlation of the genotype-phenotype relations.
Asunto(s)
Factores de Transcripción de Tipo Kruppel/genética , Mutación , Proteínas del Tejido Nervioso/genética , Síndrome de Pallister-Hall/genética , Síndrome de Pallister-Hall/historia , Autopsia , Exhumación , Expresión Génica , Genes Letales , Estudios de Asociación Genética , Historia del Siglo XX , Humanos , Recién Nacido , Masculino , Síndrome de Pallister-Hall/diagnóstico , Síndrome de Pallister-Hall/patología , Proteína Gli3 con Dedos de ZincRESUMEN
Pallister-Hall syndrome (PHS) is a rare disorder caused by mutations in GLI3 that produce a transcriptional repressor (GLI3R). Individuals with PHS present with a variably penetrant variety of urogenital system malformations, including renal aplasia or hypoplasia, hydroureter, hydronephrosis or a common urogenital sinus. The embryologic mechanisms controlled by GLI3R that result in these pathologic phenotypes are undefined. We demonstrate that germline expression of GLI3R causes renal hypoplasia, associated with decreased nephron number, and hydroureter and hydronephrosis, caused by blind-ending ureters. Mice with obligate GLI3R expression also displayed duplication of the ureters that was caused by aberrant common nephric duct patterning and ureteric stalk outgrowth. These developmental abnormalities are associated with suppressed Hedgehog signaling activity in the cloaca and adjacent vesicular mesenchyme. Mice with conditional expression of GLI3R were utilized to identify lineage-specific effects of GLI3R. In the ureteric bud, GLI3R expression decreased branching morphogenesis. In Six2-positive nephrogenic progenitors, GLI3R decreased progenitor cell proliferation reducing the number of nephrogenic precursor structures. Using mutant mice with Gli3R and Gli3 null alleles, we demonstrate that urogenital system patterning and development is controlled by the levels of GLI3R and not by an absence of full-length GLI3. We conclude that the urogenital system phenotypes observed in PHS are caused by GLI3R-dependent perturbations in nephric duct patterning, renal branching morphogenesis and nephrogenic progenitor self-renewal.
Asunto(s)
Linaje de la Célula/genética , Regulación del Desarrollo de la Expresión Génica , Hidronefrosis/genética , Riñón/anomalías , Factores de Transcripción de Tipo Kruppel/genética , Proteínas del Tejido Nervioso/genética , Síndrome de Pallister-Hall/genética , Anomalías Urogenitales/genética , Animales , Tipificación del Cuerpo/genética , Proliferación Celular , Modelos Animales de Enfermedad , Embrión de Mamíferos , Proteínas de Homeodominio/genética , Proteínas de Homeodominio/metabolismo , Humanos , Hidronefrosis/metabolismo , Hidronefrosis/patología , Riñón/metabolismo , Riñón/patología , Factores de Transcripción de Tipo Kruppel/metabolismo , Ratones , Ratones Noqueados , Mutación , Nefronas/anomalías , Nefronas/embriología , Nefronas/metabolismo , Proteínas del Tejido Nervioso/metabolismo , Síndrome de Pallister-Hall/metabolismo , Síndrome de Pallister-Hall/patología , Fenotipo , Transducción de Señal , Células Madre/metabolismo , Células Madre/patología , Factores de Transcripción/genética , Factores de Transcripción/metabolismo , Uréter/anomalías , Uréter/embriología , Uréter/metabolismo , Anomalías Urogenitales/metabolismo , Anomalías Urogenitales/patología , Proteína Gli3 con Dedos de ZincRESUMEN
Polydactyly is among comnion extremity abnormalities. Mutations of GLI3 gene have been reported commonly in Greig Cephalopolysyndactyly Syndrome (GCPS) and Pallister-Hall Syndrome (PHS). We have determined two different mutations of GLI3 gene in two different cases, one of which is with GCPS and the other one is with PHS. A deletion mutation was detected in the proband with GCPS and his mother. Otherwise, we found that, unlike the previously reported, the mutation c.2437C>T, p.Q813X which was detected in the GLI3 gene caused typical PHS. We are in thought of that our cases will contribute to understanding of phenotypic variability leading to GLI3 mutations.
Asunto(s)
Acrocefalosindactilia/genética , Análisis Mutacional de ADN , Síndrome de Pallister-Hall/genética , Proteína Gli3 con Dedos de Zinc/genética , Acrocefalosindactilia/diagnóstico , Adolescente , Ano Imperforado/diagnóstico , Ano Imperforado/genética , Variación Biológica Poblacional , Niño , Tamización de Portadores Genéticos , Asesoramiento Genético , Hamartoma/diagnóstico , Hamartoma/genética , Humanos , Imagen por Resonancia Magnética , Masculino , Síndrome de Pallister-Hall/diagnóstico , Enfermedades de la Hipófisis/diagnóstico , Enfermedades de la Hipófisis/genética , Eliminación de Secuencia/genéticaRESUMEN
Pallister-Hall syndrome is a complex malformation syndrome characterized by a wide range of anomalies including hypothalamic hamartoma, polydactyly, bifid epiglottis, and genitourinary abnormalities. It is usually caused by truncating frameshift/nonsense and splicing mutations in the middle third of GLI3. The clinical course ranges from mild to lethal in the neonatal period. We present the first patient with Pallister-Hall syndrome reported with total colonic aganglionosis, a rare form of Hirschsprung disease with poor long-term outcome. The patient also had an imperforate anus, which is the third individual with Pallister-Hall syndrome reported with both Hirschsprung disease and an imperforate anus. Molecular testing via amniocentesis showed an apparently de novo novel nonsense mutation c.2641 C>T (p.Gln881*). His overall medical course was difficult and was complicated by respiratory failure and pan-hypopituitarism. Invasive care was ultimately withdrawn, and the patient expired at three months of age. This patient's phenotype was complex with unusual gastrointestinal features ultimately leading to a unfavorable prognosis and outcome, highlighting the range of clinical severity in patients with Pallister-Hall syndrome.
Asunto(s)
Ano Imperforado/diagnóstico , Ano Imperforado/genética , Enfermedad de Hirschsprung/diagnóstico , Enfermedad de Hirschsprung/genética , Síndrome de Pallister-Hall/diagnóstico , Síndrome de Pallister-Hall/genética , Ano Imperforado/cirugía , Biopsia , Hibridación Genómica Comparativa , Resultado Fatal , Femenino , Enfermedad de Hirschsprung/cirugía , Humanos , Recién Nacido , Cariotipo , Factores de Transcripción de Tipo Kruppel/genética , Mutación , Proteínas del Tejido Nervioso/genética , Fenotipo , Embarazo , Índice de Severidad de la Enfermedad , Tomografía Computarizada por Rayos X , Ultrasonografía Prenatal , Proteína Gli3 con Dedos de ZincRESUMEN
The Pallister-Hall syndrome (PHS) was identified and described as a specific entity in the late 1970s and early 1980s. Subsequently, many patients were reported expanding the phenotype. Familial cases demonstrated variability and lead to linkage and then gene identification. Mutations in the responsible gene, GLI3 are also known to be involved in several other disorders. Genotype/phenotype correlations have led to fine mapping of GLI3 and the recognition that PHS is caused by dominant negative mutations in the middle third of the gene.
Asunto(s)
Genética Médica , Síndrome de Pallister-Hall/diagnóstico , Síndrome de Pallister-Hall/genética , Genética Médica/historia , Historia del Siglo XX , Historia del Siglo XXI , Humanos , Síndrome de Pallister-Hall/historiaRESUMEN
Greig cephalopolysyndactyly syndrome (GCPS) and isolated preaxial polydactyly type IV (PPD-IV) are rare autosomal dominant disorders, both caused by mutations in the GLI3 gene. GCPS is mainly characterised by craniofacial abnormalities (macrocephaly/prominent forehead, hypertelorism) and limb malformations, such as PPD-IV, syndactyly and postaxial polydactyly type A or B (PAPA/B). Mutations in the GLI3 gene can also lead to Pallister-Hall syndrome (PHS) and isolated PAPA/B. In this study, we investigated 16 unrelated probands with the clinical diagnosis of GCPS/PPD-IV and found GLI3 mutations in 12 (75%) of them (nine familial and three sporadic cases). We also performed a detailed clinical evaluation of all 12 GLI3-positive families, with a total of 27 patients. The hallmark triad of GCPS (preaxial polydactyly, macrocephaly/prominent forehead, hypertelorism) was present in 14 cases (52%), whereas at least one typical dysmorphic feature was manifested in 17 patients (63%). Upon sequencing of the GLI3 gene, we demonstrated eight novel and two previously reported heterozygous point mutations. We also performed multiplex ligation-dependent probe amplification (MLPA) to screen for intragenic copy number changes and identified heterozygous deletions in the two remaining cases (16.7%). Our findings fully support previous genotype-phenotype correlations, showing that exonic deletions, missense mutations, as well as truncating variants localised out of the middle third of the GLI3 gene result in GCPS/PPD-IV and not PHS. Additionally, our study shows that intragenic GLI3 deletions may account for a significant proportion of GCPS/PPD-IV causative mutations. Therefore, we propose that MLPA or quantitative polymerase chain reaction (qPCR) should be implemented into routine molecular diagnostic of the GLI3 gene.
Asunto(s)
Acrocefalosindactilia/genética , Estudios de Asociación Genética/métodos , Factores de Transcripción de Tipo Kruppel/genética , Proteínas del Tejido Nervioso/genética , Mutación Puntual , Polidactilia/genética , Acrocefalosindactilia/diagnóstico , Adolescente , Adulto , Niño , Preescolar , Variaciones en el Número de Copia de ADN , Pruebas Genéticas/métodos , Heterocigoto , Humanos , Lactante , Factores de Transcripción de Tipo Kruppel/metabolismo , Masculino , Persona de Mediana Edad , Mutación Missense , Proteínas del Tejido Nervioso/metabolismo , Síndrome de Pallister-Hall/genética , Linaje , Polidactilia/diagnóstico , Reacción en Cadena en Tiempo Real de la Polimerasa/métodos , Pulgar/anomalías , Adulto Joven , Proteína Gli3 con Dedos de ZincRESUMEN
A range of phenotypes including Greig cephalopolysyndactyly and Pallister-Hall syndromes (GCPS, PHS) are caused by pathogenic mutation of the GLI3 gene. To characterize the clinical variability of GLI3 mutations, we present a subset of a cohort of 174 probands referred for GLI3 analysis. Eighty-one probands with typical GCPS or PHS were previously reported, and we report the remaining 93 probands here. This includes 19 probands (12 mutations) who fulfilled clinical criteria for GCPS or PHS, 48 probands (16 mutations) with features of GCPS or PHS but who did not meet the clinical criteria (sub-GCPS and sub-PHS), 21 probands (6 mutations) with features of PHS or GCPS and oral-facial-digital syndrome, and 5 probands (1 mutation) with nonsyndromic polydactyly. These data support previously identified genotype-phenotype correlations and demonstrate a more variable degree of severity than previously recognized. The finding of GLI3 mutations in patients with features of oral-facial-digital syndrome supports the observation that GLI3 interacts with cilia. We conclude that the phenotypic spectrum of GLI3 mutations is broader than that encompassed by the clinical diagnostic criteria, but the genotype-phenotype correlation persists. Individuals with features of either GCPS or PHS should be screened for mutations in GLI3 even if they do not fulfill clinical criteria.