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Health Dictionary

Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.

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Chromosome 1, deletion q21 q25

Introduction

Overview

Overview

A rare chromosomal disorder where deletion of a portion of chromosome 1 results in various abnormalities such as retarded fetal growth, facial anomalies, osteoporosis, mental retardation and hearing loss.[1]

References

References

  1. ↑ Beemer FA, Klep-de Pater JM, Sepers GJ, Janssen B (1985). “Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21—-q25) and del(1)(q41—-q43)”. Clin. Genet. 27 (5): 515–9. PMID 4006278. Unknown parameter |month= ignored (help)

Template:WikiDoc Sources

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Cafer Zorkun, M.D., Ph.D. [2], Raviteja Guddeti, M.B.B.S.[3]