Homozygous Mutation in the FANCD2 Gene Observed in a Saudi Male Infant with Severe Ambiguous Genitalia

Homozygous Mutation in the FANCD2 Gene Observed in a Saudi Male Infant with Severe Ambiguous Genitalia

Fanconi anemia (FA) is a rare autosomal recessive inherited disease caused by gene mutations that are primarily involved in the response to or repair of DNA damage. FA characterizes by multiple congenital abnormalities and malformations including growth retardation, renal agenesis, absence of radial...

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Dades bibliogràfiques
Autors principals:	Aida Al Jabri, Nusaybah Al Naim, Abeer Al Dossari
Format:	Article
Idioma:	English
Publicat:	Hindawi Limited 2021-01-01
Col·lecció:	Case Reports in Endocrinology
Accés en línia:	http://dx.doi.org/10.1155/2021/6686312

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