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RSS FeedsIdentification of a novel KAT6A variant in an infant presenting with facial dysmorphism and developmental delay: a case report and literature review (BMC Medical Genomics)

 
 

20 december 2021 20:39:55

 
Identification of a novel KAT6A variant in an infant presenting with facial dysmorphism and developmental delay: a case report and literature review (BMC Medical Genomics)
 


Arboleda-Tham syndrome (ARTHS), caused by a pathogenic variant of KAT6A, is an autosomal dominant inherited genetic disorder characterized by various degrees of developmental delay, dysmorphic facial appearance, ...


 
156 viewsCategory: Genomics, Medicine
 
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X-linked sideroblastic anaemia in a female fetus: a case report and a literature review (BMC Medical Genomics)
 
 
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