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PMID: 3096136 Published · ppublish English Case Reports Journal Article

Interstitial 7q deletion [46,XY,del (7) (pter----cen::q112----qter)] in a retarded quadriplegic boy with normal beta glucuronidase.

American journal of medical genetics ·Vol. 25 ·No. 2 ·1986-10-00 ·Pages 245-9

Frydman M, Steinberger J, Shabtai F, Steinherz R

Abstract

A 14-year-old severely retarded male with deletion of chromosomal band 7 cen----q112 is described. Clinical features include short stature, microcephaly, unusual facies with narrow forehead, short nose, malar hypoplasia, protruding alveolar ridges and incisors, receding chin, relatively long philtrum, and large ears. In addition, he had bilateral inguinal herniae cryptorchidism with hypogonadism, pulmonic stenosis, and spastic quadriplegia. Normal activity of beta-glucuronidase was found in the patient's leukocytes. This finding suggests that the gene is not in the deleted region, narrowing the smallest region of overlap to 7q112----q22.

MeSH Terms
Abnormalities, Multiple/enzymology,genetics Adolescent Chromosome Deletion Chromosomes, Human, Pair 7 Genetic Markers Glucuronidase/blood,genetics Humans Intellectual Disability/enzymology,genetics Male Quadriplegia/enzymology,genetics beta-Galactosidase/genetics
Chemicals
Genetic Markers beta-Galactosidase Glucuronidase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Frydman M
Steinberger J
Shabtai F
Steinherz R
Article Info
Journal
American journal of medical genetics
Abbr.
Am J Med Genet
ISSN
0148-7299
Published
1986-10-00
Pages
245-9
Language
English
Region
United States
NLM ID
7708900
Subset
IM
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