Chromosome 1- monosomy 1q25 q32
Overview
A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as digital defects, facial dysmorphism, retarded growth, mental retardation and spasticity.
Symptoms
* Small ear lobe * Underdeveloped ear lobe * Short head * Broad great toe * Bifid great toe * Short foot * Short toes * Curved fifth finger * Spasticity * Rigidity * Underdeveloped antihelix * Abnormal antihelix * Fetal growth retardation * Large fontanelle * Low-set ears * Mental retardation * Small head * Broad thumb * Bifid thumb * Round face * Small jaw * Short neck * Short stature * Delayed bone age * Fine hair * Increased muscle tone * Short nose * Small nose * Sparse scalp hair * Absent scalp hair * Congenital heart anomaly
Diagnosis
This medical information about signs and symptoms for Chromosome 1, monosomy 1q25 q32 has been gathered from various sources, may not be fully accurate, and may not be the full list of Chromosome 1, monosomy 1q25 q32 signs or Chromosome 1, monosomy 1q25 q32 symptoms. Furthermore, signs and symptoms of Chromosome 1, monosomy 1q25 q32 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 1, monosomy 1q25 q32 symptoms.