Chromosome 16- uniparental disomy
Overview
A rare chromosomal disorder where an extra copy of chromosome 16 is inherited from one parent only.
Symptoms
* Retarded fetal growth * Stillbirth * Low birth weight * Premature membrane rupture during pregnancy
Diagnosis
This medical information about signs and symptoms for Chromosome 16, uniparental disomy has been gathered from various sources, may not be fully accurate, and may not be the full list of Chromosome 16, uniparental disomy signs or Chromosome 16, uniparental disomy symptoms. Furthermore, signs and symptoms of Chromosome 16, uniparental disomy may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Chromosome 16, uniparental disomy symptoms.