Arachnodactyly-intellectual disability-dysmorphism syndrome

MONDO:0015235

Arachnodactyly-intellectual disability-dysmorphism syndrome is characterized by moderate intellectual deficit, brachycephaly, typical facies (thin lips and microstomia), ectomorphic habitus with extremely long, thin fingers and toes, and hypoplastic external genitalia. It has been described in three patients.

Also known as: De Die-Smulders-Vles-Fryns syndrome, die Smulders Vles Fryns syndrome, arachnodactyly - intellectual disability - dysmorphism

0 clinical trials for this condition and its sub-types, 0 tagged with Arachnodactyly-intellectual disability-dysmorphism syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Syndromic disease (7133) ↑ Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome (90)

Including sub-types (0) Tagged with Arachnodactyly-intellectual disability-dysmorphism syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.