You are using an outdated browser. Please upgrade your browser to improve your experience.

Alkuraya-Kucinskas syndrome

Disease Summary
Associated Targets (1)
Tbio

1


Explore Associated Targets
Uniprot Description An autosomal recessive syndrome characterized by brain atrophy and arthrogryposis. Patients present with cerebral parenchymal underdevelopment, lissencephaly, severe to mild ventriculomegaly, and cerebellar hypoplasia with brainstem dysgenesis. Most affected individuals die in utero or soon after birth. The few patients who survive have variable intellectual disability and may have seizures. Facial dysmorphism, cardiac and ophthalmologic anomalies, such as microphthalmia and cataract, are additional features.
Mondo Term and Equivalent IDs
MONDO:0060631:  Alkuraya-Kucinskas syndrome
DOID:0111555: 
UMLS:CN737163: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)