RESUMEN
Conradi-Hünermann-Happle syndrome (CHHS) is a rare genodermatosis resulting from mutations in the EBP (emopamil binding protein) gene. Dermatologic manifestations may include cicatricial alopecia, ichthyosis, follicular atrophoderma, pigmentary abnormalities, and nail dystrophy. In addition to genetic testing and clinical findings, trichoscopic findings may aid in the diagnosis. In this case report, we discuss the trichoscopic findings in a 3-year-old girl with CHHS and how these findings help us understand the pathophysiology of this disease.
Asunto(s)
Condrodisplasia Punctata , Ictiosis , Anomalías Cutáneas , Femenino , Humanos , Preescolar , Alopecia/diagnóstico , Alopecia/genética , Mutación , Condrodisplasia Punctata/diagnóstico , Condrodisplasia Punctata/genéticaRESUMEN
Conradi-Hünermann-Happle syndrome is rare X-linked dominant syndrome associated with stippled epiphyseal calcifications, congenital cataracts, Blaschkoid ichthyosiform scaling, and follicular atrophoderma. This case describes a novel finding of hypocalcemia and hypoparathyroidism in an infant with Conradi-Hünermann-Happle syndrome.
Asunto(s)
Condrodisplasia Punctata , Hipocalcemia , Condrodisplasia Punctata/complicaciones , Condrodisplasia Punctata/diagnóstico , Condrodisplasia Punctata/genética , Humanos , Hipocalcemia/complicaciones , Hipocalcemia/diagnóstico , Hipocalcemia/tratamiento farmacológico , Lactante , Recién NacidoRESUMEN
We describe a female infant with X-linked chondrodysplasia punctata (CDPX1) as a result of maternal isodisomy of the X chromosome. Targeted Sanger sequencing and targeted next-generation sequencing of ARSL were used to test for the familial variant. This patient was homozygous for ARSL NM_000047.2: c.1227_1228delinsAT p.(Ser410Cys) familial variant, consistent with a diagnosis of CDPX1. Uniparental disomy is a type of chromosomal variation. Although not necessarily pathogenic, it can cause imprinting disorders and X-linked recessive disorders in females, and be a cause of autosomal recessive conditions when only one parent is a carrier. The patient described highlights that uniparental disomy can be a rare cause of X-linked recessive conditions. This mode of inheritance has not been previously described in this condition.
Asunto(s)
Condrodisplasia Punctata , Enfermedades Genéticas Ligadas al Cromosoma X , Condrodisplasia Punctata/diagnóstico , Condrodisplasia Punctata/genética , Femenino , Homocigoto , Humanos , Lactante , Disomía Uniparental/genéticaRESUMEN
Congenital combined vitamin K-dependent clotting factors deficiency (VKCFD) is a rare autosomal recessive disease resulting in hemorrhagic symptoms usually associated with developmental disorders and bone abnormalities. Pathogenic variants in two genes encoding enzymes of the vitamin K cycle, GGCX and VKORC1, can lead to this disorder. We present the case of a male fetus with a brachytelephalangic chondrodysplasia punctata (CDP), absence of nasal bone, growth restriction, and bilateral ventriculomegaly at 18 weeks of gestation. Pathological examination showed a Binder phenotype, hypoplastic distal phalanges, stippled epiphyses, and brain abnormalities suggestive of a brain hemorrhage. Two GGCX pathogenic variants inherited respectively from the mother and the father were identified. To our knowledge, this is the first prenatal description of VKCFD. Even if it remains a rare etiology, which is mostly described in children or adult patients, VKCFD should be considered in fetuses with CDP.
Asunto(s)
Ligasas de Carbono-Carbono , Condrodisplasia Punctata , Factores de Coagulación Sanguínea , Ligasas de Carbono-Carbono/genética , Condrodisplasia Punctata/diagnóstico , Condrodisplasia Punctata/genética , Femenino , Feto , Humanos , Masculino , Embarazo , Vitamina K , Vitamina K 1 , Vitamina K Epóxido Reductasas/genéticaRESUMEN
A 4-year-old girl presented with congenital patches of scalp alopecia, which on physical examination, was consistent with blaschkolinear alopecic patches with mild epidermal atrophy. Similar atrophic hypopigmented patches were seen on the trunk and proximal extremities. With the clinical suspicion of Conradi-Hünermann-Happle syndrome, genetic testing was performed and revealed a mutation in the EBP gene. Despite characteristic cutaneous findings, no skeletal, ocular, or other anomalies were found on further evaluation.
Asunto(s)
Condrodisplasia Punctata , Anomalías Cutáneas , Alopecia , Preescolar , Condrodisplasia Punctata/diagnóstico , Condrodisplasia Punctata/genética , Ojo , Cara , Femenino , HumanosRESUMEN
Conradi-Hünermann-Happle Syndrome, also called X-linked rhizomelic chondrodysplasia punctata, is a rare genodermatosis that presents with cutaneous, skeletal, and ophthalmological abnormalities. Herein, we report a full-term newborn that presented at birth with scattered blaschkolinear bands of adherent scales and scalp erosions in a spiral distribution. Genetic analysis of emopamil-binding protein gene revealed a previously undescribed heterozygous mutation of c.333delC.
Asunto(s)
Condrodisplasia Punctata/genética , Piel/patología , Esteroide Isomerasas/genética , Alopecia/genética , Alopecia/patología , Condrodisplasia Punctata/diagnóstico , Condrodisplasia Punctata/patología , Femenino , Humanos , Recién Nacido , Espectrometría de Masas , FenotipoRESUMEN
Rhizomelic chondrodysplasia punctata is a rare, often fatal disease that shares many clinical dysmorphologic features with the rare often non-lethal chondrodysplasia punctata due to maternal autoimmune disease. Characteristic findings of both conditions include mid-face hypoplasia, stippled epiphyses of the vertebrae and long bones, and growth failure. A growing association with anti-ribonucleoprotein antibodies is emerging amongst patients with chondrodysplasia punctata due to maternal autoimmune disease and also neonatal lupus that have potential important screening implications. We present a unique case of chondrodysplasia punctata with neonatal lupus in the setting of positive anti-RNP antibodies and negative anti-Ro/SSA and -La/SSB antibodies born to a mother with mixed connective tissue disease and Raynaud's syndrome.
Asunto(s)
Condrodisplasia Punctata , Lupus Eritematoso Sistémico/congénito , Anticuerpos Antinucleares , Condrodisplasia Punctata/diagnóstico , Femenino , Humanos , Lactante , Recién Nacido , MadresRESUMEN
Our improved tools to identify the aetiologies in patients with multiple abnormalities resulted in the finding that some patients have more than a single genetic condition and that some of the diagnoses made in the past are acquired rather than inherited. However, limited knowledge has been accumulated regarding the phenotypic outcome of the interaction between different genetic conditions identified in the same patients. We report a newborn girl with brachytelephalangic chondrodysplasia punctata (BCDP) as well as frontonasal dysplasia, ptosis, bilateral hearing loss, vertebral anomalies, and pulmonary hypoplasia who was found, by whole exome sequencing, to have a de novo pathogenic variant in RAF1 (c.770C>T, [p.Ser257Leu]) and a likely pathogenic variant in SIX2 (c.760G>A [p.A254T]), as well as maternal systemic lupus erythematosus (SLE). This case shows that BCDP is most probably not a diagnostic entity and can be associated with various conditions associated with CDP including maternal SLE.
Asunto(s)
Anomalías Múltiples/genética , Condrodisplasia Punctata/genética , Proteínas de Homeodominio/genética , Proteínas del Tejido Nervioso/genética , Proteínas Proto-Oncogénicas c-raf/genética , Anomalías Múltiples/diagnóstico , Anomalías Múltiples/patología , Condrodisplasia Punctata/diagnóstico , Condrodisplasia Punctata/patología , Anomalías Craneofaciales/diagnóstico , Anomalías Craneofaciales/genética , Anomalías Craneofaciales/patología , Cara/anomalías , Cara/patología , Femenino , Predisposición Genética a la Enfermedad , Hernia Diafragmática/diagnóstico , Hernia Diafragmática/genética , Humanos , Recién NacidoRESUMEN
RATIONALE: X-linked dominant chondrodysplasia punctata type 2 (CDPX2) is a condition involving facial, skin, and skeletal dysplasia as a result of a mutation in emopamil binding protein (EBP). It usually presents with mild symptoms in female patients but is fatal in male patients. PATIENT CONCERNS: A fetus was diagnosed with asymmetrical short limbs and a narrow and small thorax by prenatal ultrasound examination at 24+5 weeks gestation. The pregnancy was terminated at 27 weeks of gestation; gross examination, postnatal X-ray and, whole exome analysis were performed to clarify the diagnosis. DIAGNOSIS: A provisional diagnosis of fatal skeletal dysplasia was given and the definite diagnosis of CDPX2 was based on postnatal X-ray and genetic testing of the aborted fetus. INTERVENTION: The pregnancy was terminated at 27 weeks' gestation after a fetal ultrasound indicated a severe abnormal phenotype. OUTCOMES: Whole exome analysis of aborted tissue confirmed EBP mutation in this case. Unlike most case reports, this female patient presented a severe phenotype that was considered to be related to X-chromosome inactivation. LESSONS: Chondrodysplasia punctata (CDP) should be considered if prenatal ultrasound shows high punctuate echoes at the metaphysis of long bones and asymmetrical short lower limbs. Postnatal X-ray and measurement of sterol levels in the amniotic fluid may aid in the diagnosis of CDP, but the condition can be confirmed with genetic testing of a blood sample or aborted tissue after delivery.
Asunto(s)
Condrodisplasia Punctata/diagnóstico , Condrodisplasia Punctata/genética , Femenino , Humanos , Fenotipo , Embarazo , Ultrasonografía PrenatalAsunto(s)
Anomalías Maxilofaciales/diagnóstico , Diagnóstico Prenatal , Condrodisplasia Punctata/diagnóstico , Condrodisplasia Punctata/diagnóstico por imagen , Condrodisplasia Punctata/genética , Diagnóstico Diferencial , Femenino , Humanos , Imagen por Resonancia Magnética , Anomalías Maxilofaciales/diagnóstico por imagen , Anomalías Maxilofaciales/genética , Fenotipo , Embarazo , Tercer Trimestre del Embarazo , Ultrasonografía Prenatal , Adulto JovenRESUMEN
Chondrodysplasia punctate (CDP) is a rare group of disorders with both genetic and non-genetic underlying aetiologies. The genetic causes associated with CDP include peroxisomal disorders, type two mucolipidosis, type 3 mucopolysaccharidosis, GM1 gangliosidosis and chromosomal disorders. Peroxisomal disorders include deficiency of dihydroxyacetone phosphate acyltransferase, encoded by GNPAT, deficiency of the peroxisomal enzyme alkyl-dihydroxyacetone phosphate synthase, encoded by AGPS and Zellweger syndrome. The chromosomal disorders include Turner syndrome, trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome) and trisomy 9. Among non-genetic causes, teratogen exposure like warfarin and acenocoumarol is well known but for the past few years cases have been reported with maternal autoimmune disease mainly systemic lupus erythematosus and rarely with mixed connective tissue disorder (MCTD). However, the exact mechanism for the occurrence of CDP in MCTD is still unknown. We present here a 35-week appropriate for gestational age baby born to a second gravid mother, a known case of MCTD on treatment with hydroxychloroquine. The baby had mid-facial hypoplasia and bilateral talar region punctuate calcification suggestive of chondrodysplasia punctata. Global data on such cases are very scant. Further research work is needed to explore the association of specific antibody titre with the occurrence of such condition in maternal autoimmune disease.
Asunto(s)
Condrodisplasia Punctata/diagnóstico , Enfermedad Mixta del Tejido Conjuntivo , Complicaciones del Embarazo , Adulto , Diagnóstico Diferencial , Femenino , Humanos , Recién Nacido , EmbarazoAsunto(s)
Condrodisplasia Punctata/genética , Anomalías Craneofaciales/genética , Intestinos/anomalías , Mosaicismo , Mutación , Anomalías Cutáneas/genética , Receptor Smoothened/genética , Sindactilia/genética , Adulto , Condrodisplasia Punctata/diagnóstico , Anomalías Craneofaciales/diagnóstico , Análisis Mutacional de ADN , Predisposición Genética a la Enfermedad , Humanos , Masculino , Fenotipo , Anomalías Cutáneas/diagnóstico , Sindactilia/diagnósticoRESUMEN
Chondrodysplasia punctata is a group of congenital bone and cartilage disorders characterized by erratic calcification during development. Laryngeal and tracheal calcification and subsequent stenosis, while being reported in several cases of chondrodysplasia punctata, are not frequent findings and there are no proposed management techniques. We describe here a case of an infant with chondrodysplasia punctata associated to tracheal stenosis that was successfully treated with balloon dilation, and with long term follow-up.
Asunto(s)
Condrodisplasia Punctata/diagnóstico , Estenosis Traqueal/etiología , Condrodisplasia Punctata/complicaciones , Humanos , Lactante , MasculinoRESUMEN
This manuscript presents a molecularly demonstrated gonadal mosaicism from paternal origin for X-linked dominant chondrodysplasia punctata by single sperm typing. A couple who had experienced two medical terminations of pregnancy of female fetuses was referred to our pre-implantation genetic diagnosis (PGD) centre with the diagnosis of maternally derived gonadal mosaicism. Indeed, genetic analyses of different DNA samples - including semen - from the healthy parents failed to detect the variant found in the fetuses. Six embryos, all male, were obtained during the PGD cycle. The causative variant was not detected in any embryo, whereas five embryos had inherited the 'at-risk' maternal haplotype. The assumption of a maternal gonadal mosaicism was still possible, but this finding allowed us to consider the possibility of a paternal rather than maternal gonadal mosaicism. It prompted us to perform extensive single sperm analyses, demonstrating a low-frequency paternal germline mosaicism, which led to completely different haplotype phasing and PGD counselling. In conclusion, this case further exemplifies that germline mosaicism is a pitfall in PGD where diagnosis largely relies on linkage analysis and suggests that tracing the parental inheritance through polar body analysis and/or single sperm typing experiments is of major importance for adequate genetic counselling and accurate PGD. © 2016 John Wiley & Sons, Ltd.
Asunto(s)
Condrodisplasia Punctata/diagnóstico , Enfermedades Genéticas Ligadas al Cromosoma X/diagnóstico , Mosaicismo , Herencia Paterna/genética , Diagnóstico Preimplantación , Análisis de la Célula Individual/métodos , Espermatozoides/metabolismo , Adulto , Condrodisplasia Punctata/genética , Errores Diagnósticos , Femenino , Enfermedades Genéticas Ligadas al Cromosoma X/genética , Pruebas Genéticas/métodos , Células Germinativas , Humanos , Masculino , Herencia Materna/genética , Linaje , Embarazo , Diagnóstico Preimplantación/métodos , Diagnóstico Preimplantación/normas , Recurrencia , Espermatozoides/citologíaRESUMEN
Conradi-Hünermann-Happle syndrome, or X-linked dominant chondrodysplasia punctata type 2 (CDPX2), is a genodermatosis caused by mutations in EBP. While typically lethal in males, females with CDPX2 generally manifest by infancy or childhood with variable features including congenital ichthyosiform erythroderma, chondrodysplasia punctata, asymmetric shortening of the long bones, and cataracts. We present a 36-year-old female with short stature, rhizomelic and asymmetric limb shortening, severe scoliosis, a sectorial cataract, and no family history of CDPX2. Whole exome sequencing (WES) revealed a p.Arg63del mutation in EBP, and biochemical studies confirmed a diagnosis of CDPX2. Short stature in combination with ichthyosis or alopecia, cataracts, and limb shortening in an adult should prompt consideration of a diagnosis of CDPX2. As in many genetic syndromes, the hallmark features of CDPX2 in pediatric patients are not readily identifiable in adults. This demonstrates the utility of WES as a diagnostic tool in the evaluation of adults with genetic disorders.
Asunto(s)
Alopecia/genética , Secuencia de Bases , Catarata/genética , Condrodisplasia Punctata/genética , Enanismo/genética , Eliminación de Secuencia , Esteroide Isomerasas/genética , Adulto , Negro o Afroamericano , Alopecia/diagnóstico , Alopecia/patología , Catarata/diagnóstico , Catarata/patología , Condrodisplasia Punctata/diagnóstico , Condrodisplasia Punctata/patología , Enanismo/diagnóstico , Enanismo/patología , Exoma , Femenino , Genes Ligados a X , Humanos , Datos de Secuencia Molecular , Esteroide Isomerasas/deficienciaRESUMEN
Calcification of the airways is rarely seen in children. A male baby was born at 34 weeks with severe respiratory distress. Intubation was difficult with severe hypercarbia after intubation. Chest radiography demonstrated calcification in the tracheobronchial tree and this was confirmed with Chest CT scan. Flexible bronchoscopy confirmed long-segment funnel tracheal stenosis with visible calcifications in the trachea and bronchi. Chondrodysplasia punctata was diagnosed based on the clinical and radiological findings.