X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome

From WikiMD's WELLNESSPEDIA

Alternate names

PRS; MRXS2; Prieto syndrome; Prieto-Badia-Mulas syndrome

Definition

An X-linked syndromic intellectual disability characterized by intellectual disability, subcortical cerebral atrophy, dental anomalies, patella luxation, lower back skin dimple, and dysmorphic facial features.

Epidemiology

It has been described in eight males from multiple generations of one family.

Cause

The locus for the causative gene for this syndrome has been localised to the region between p11.22 and p21.1 on the X chromosome.

Signs and symptoms

For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed.

30%-79% of people have these symptoms

Diagnosis

Treatment

NIH genetic and rare disease info

X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome is a rare disease.


Resources

Message
No content specified




<html><link rel="canonical" href="https://wikimd.com/wiki/X-linked+intellectual+disability-dysmorphism-cerebral+atrophy+syndrome">‎ <meta name=”viewport” content=”width=device-width, initial-scale=1″> </html>