Gabriele-de Vries syndrome

Orpha code: 506358OMIM code: 617557

Definicja

A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by variable developmental delay and intellectual disability, movement disorder or gait abnormalities, and dysmorphic craniofacial features (such as facial asymmetry, broad forehead, posteriorly rotated ears, thick lower lip, micrognathia, or cleft palate). A variety of congenital malformations have been reported in addition, including ocular, renal, cardiac, and joint anomalies, among others. Some patients show behavioral alterations (autism, hyperactivity, or anxiety).

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
YY1 haploinsufficiency syndrome
Zespół haploinsuficjencji YY1
Kod ORPHA
506358
Kod OMIM
617557
Kod ICD10
-
Kod ICD11
-

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl