Opis choroby * EnglishPolish Pobierz sekcję do PDF Definicja A rare multiple congenital anomalies syndrome usually characterized by microcephaly, ocular anomalies such as microphthalmia, and apple-peel intestinal atresia. Facial dysmorphism is reported in some cases and may include narrow or sloped forehead, hypertelorism, microphthalmia, dysplastic, edematous deep-set eyes, short palpebral fissures, large or low set ears, broad nasal root, anteverted or broad nasal tip, long philtrum, micrognathia, thin upper vermillion, large mouth and skin tag on the cheek. Motor delay and intellectual disability have been reported. Heart, brain, craniofacial abnormalities, renal hypoplasia and other anomalies (e.g. lower limb edema, thrombocytopenia) are variably present. Rarely, cases without intestinal atresia, microcephaly or developmental delay can be found. Severe lethal cases have also been reported. Dane Klasyfikacja Zespół wad wrodzonych Synonimy Apple-peel intestinal atresia-ocular anomalies-microcephaly syndrome Jejunal atresia-microcephaly-ocular anomalies syndrome Apple-peel intestinal atresia-ocular anomalies-microcephaly syndrome Jejunal atresia-microcephaly-ocular anomalies syndrome Kod ORPHA 506307 Kod OMIM 243605 Kod ICD10 Q13.8 Kod ICD11 - *Źródło Rozszerzony opis choroby Pobierz sekcję do PDF Brak opisu rozszerzonego dla tej choroby. Opracowanie w toku. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl