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First reported cases with Xia-Gibbs syndrome from India harboring novel variants in AHDC1.
Danda, Sumita; Datar, Chaitanya; Kher, Archana; Deshpande, Tanmay; Thomas, Maya Mary; Oommen, Samuel P.
Afiliación
  • Danda S; Department of Medical Genetics, Christian Medical College and Hospital, Vellore, India.
  • Datar C; Department of Paediatrics, Genetics Unit, Bharati Vidyapeeth Medical College and Hospital, Pune, India.
  • Kher A; Department of Paediatrics, Genetics Unit, Bharati Vidyapeeth Medical College and Hospital, Pune, India.
  • Deshpande T; Department of Paediatrics, Genetics Unit, Bharati Vidyapeeth Medical College and Hospital, Pune, India.
  • Thomas MM; Department of Paediatric Neurology, Christian Medical College and Hospital, Vellore, India.
  • Oommen SP; Department of Developmental Paediatrics, Christian Medical College and Hospital, Vellore, India.
Am J Med Genet A ; 188(8): 2501-2504, 2022 08.
Article en En | MEDLINE | ID: mdl-35596688
We report here two girls from different Indian families identified with novel variants in the AT Hook DNA Binding Motif Containing 1 gene (AHDC1) causing Xia-Gibbs syndrome. The diagnosis was made by clinical exome in both cases. Inconsistent dysmorphic features such as dolichocephaly in the first patient and brachycephaly in the second were observed. Prominent jaw and gelastic seizures were other features of patient 1. Thus, this syndrome, with developmental delay, poor expressive language and overlapping clinical phenotype requires the utility of next generation sequencing for diagnostic confirmation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Múltiples / Craneosinostosis / Apnea Obstructiva del Sueño / Discapacidad Intelectual / Anomalías Musculoesqueléticas Tipo de estudio: Diagnostic_studies Límite: Child / Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: India Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Múltiples / Craneosinostosis / Apnea Obstructiva del Sueño / Discapacidad Intelectual / Anomalías Musculoesqueléticas Tipo de estudio: Diagnostic_studies Límite: Child / Humans Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: India Pais de publicación: Estados Unidos