Chromosome 1- monosomy 1q32 q42
Overview
A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as fetal or newborn death, facial dysmorphism, short stature, finger defects and various other anomalies.
Symptoms
* Short stature * Short nose * Small nose * Short neck * Stillbirth * Small jaw * Short head * Cleft palate * Curved fifth finger * Depressed nasal bridge * Abnormal ear shape * Abnormal ear structure * High vaulted palate * Narrow palate * Wide set eyes * Fetal growth retardation * Low-set ears * Small eyes * Joint anomaly * Infant death * Anteverted nostrils * Malplaced anus * Small head * Thin lips
Diagnosis
This medical information about signs and symptoms for Chromosome 1, monosomy 1q32 q42 has been gathered from various sources, may not be fully accurate, and may not be the full list of Chromosome 1, monosomy 1q32 q42 signs or Chromosome 1, monosomy 1q32 q42 symptoms. Furthermore, signs and symptoms of Chromosome 1, monosomy 1q32 q42 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 1q32 q42 symptoms.