Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare multiple congenital anomalies/dysmorphic syndrome characterized by microcephaly, developmental delay and intellectual disability, postnatal growth retardation, dysmorphic craniofacial features (including sloping forehead, beaked nose, large and protruding ears, micrognathia, high-arched palate, and craniosynostosis), immunologic abnormalities with transient hypogammaglobulinemia in infancy and defective chemotaxis leading to recurrent infections, as well as autoimmune/autoinflammatory phenomena. Skeletal anomalies and hypogonadism have also been reported. Disease data Klasyfikacja Malformation syndrome Synonimy Microcephaly-hypogammaglobulinemia-abnormal immunity syndrome Małogłowie - hipogammaglobulinemia - nieprawidłowa odporność Kod ORPHA 3132 Kod OMIM 251240 Kod ICD10 Q87.8 Kod ICD11 4A01.0Y *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl