Acrofacial dysostosis Catania type
Alternate names[edit]
AFD Catania type; ACD; Opitz Mollica Sorge syndrome
Definition[edit]
A very rare acrofacialdysostosis characterized by mild intrauterine growth retardation (IUGR), postnatal short stature, microcephaly, widow's peak, mandibulofacial dysostosis without cleft palate, frequent caries, mild pre- and postaxial limb hypoplasia with brachydactyly, mild interdigital webbing, simian creases, inguinal hernia and cryptorchidism and hypospadias in males.
NIH genetic and rare disease info[edit]
Acrofacial dysostosis Catania type is a rare disease.
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Rare diseases - Acrofacial dysostosis Catania type
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