1. Mendelian
  2. Rare Diseases
  3. CHROMOSOME 15q13.3 DELETION SYNDROME

15q13.3 Microdeletion Syndrome

Table of contents:

Description

15q13.3 microdeletion (microdel15q13.3) syndrome is characterized by a wide spectrum of neurodevelopmental disorders with no or subtle dysmorphic features.

Clinical Features

Phenotypes and symptoms related to 15q13.3 Microdeletion Syndrome

  • Seizures
  • Schizophrenia
  • Bipolar affective disorder

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Alternative names

15q13.3 Microdeletion Syndrome Is also known as del(15)(q13.3), chromosome 15q13.3 microdeletion syndrome, monosomy 15q13.3.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Sources and references

You can check the following sources for additional information.

MESH Genetic Syndrome Finder

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