Gabriele-de Vries syndrome

Orpha code: 506358OMIM code: 617557

Definition

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
Classification

Malformation syndrome

Synonyms
YY1 haploinsufficiency syndrome
Zespół haploinsuficjencji YY1
ORPHA code
506358
OMIM code
617557
ICD10 code
-
ICD11 code
-

No additional description.

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