J Korean Pediatr Soc.  1995 Feb;38(2):240-244.

G Deletion Syndrome II

Affiliations
  • 1Department of Pediatrics, College of Medicine, Pusan National University, Pusan, Korea.

Abstract

We experienced a case of G deletion syndrome II in a 8 year and 1 month old boy. He showed mental retardation, microcephaly, high arched palate, low set malformed ears, epicanthal fold, thoracic deformity, tracheomegaly and two lumens of esophagus. Chromosomal study showed the deletion of long arm of chromosome 22, kariotypically he was depicted as 46, XY, 22q-. A brief review of literature was also presented.

Keyword

G deletion syndrome II

MeSH Terms

Arm
Chromosomes, Human, Pair 22
Congenital Abnormalities
Ear
Esophagus
Humans
Infant, Newborn
Intellectual Disability
Male
Microcephaly
Palate
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