Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja Distal monosomy 7q36 is a rare chromosomal anomaly syndrome, resulting from a partial deletion of the long arm of chromosome 7, with a highly variable phenotype typically characterized by holoprosencephaly, growth restriction, developmental delay, facial dysmorphism (facial clefts, prominent forehead, hypertelorism, low-set ears, flat and broad nasal bridge, large mouth), abnormal fingers and palm or sole creases, ocular abnormalities, and other congenital malformations (incl. genital anomalies and caudal deficiency sequence). Cardiopathies have been occasionally reported. Disease data Klasyfikacja Malformation syndrome Synonimy Distal deletion 7q36 Dystalna delecja 7q36 Monosomia 7qter Telomerowa delecja 7q36 Monosomy 7qter Telomeric deletion 7q36 Kod ORPHA 1636 Kod OMIM - Kod ICD10 Q93.5 Kod ICD11 - *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