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PMID: 963439 Published · ppublish English Journal Article

Use of creatine kinase for detecting severe X-linked muscular dystrophy carriers.

British medical journal ·Vol. 2 ·No. 6035 ·1976-09-04 ·Pages 577-9

Dennis NR, Evans K, Clayton B, Carter CO

Abstract

Women thought to be at risk of being carriers of Duchenne muscular dystrophy were given "odds" against their having an affected child. These were calcuated from a combination of the genetic risk from the family history and an estimation of the biochemical risk from measuring the serum creatine kinase concentration. The women were told the actual risk estimate and it was put into perspective for them as a high, medium, or low risk. Of 25 women at high risk six have had children, all girls; the two in the medium-risk group have had no children; and the 46 women at low risk have had 19 boys and 25 girls. None of the boys has the disease. With detailed counselling most potential carriers of this disease reach decisions in child bearing that are in line with their degree of risk.

MeSH Terms
Creatine Kinase/blood Female Genetic Counseling Humans Male Muscular Dystrophies/diagnosis,enzymology,genetics Pregnancy Risk Sex Chromosomes
Chemicals
Creatine Kinase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Dennis N R
Evans K
Clayton B
Carter C O
References (5)
5 references, click to expand
  1. Progressive Muscular Dystrophy. V. The Identification of the Carrier State in the Duchenne Type by Serum Creatine Kinase Determination.
    Am J Hum Genet. 1963 Jun;15(2):133-54 PMID: 17948483
  2. CREATINE KINASE LEVELS IN WOMEN WHO CARRY GENES FOR THREE TYPES OF MUSCULAR DYSTROPHY.
    Br Med J. 1965 Mar 20;1(5437):750-3 PMID: 14248444
  3. Genetic counselling in X-linked muscular dystrophy.
    J Neurol Sci. 1969 May-Jun;8(3):579-87 PMID: 4185251
  4. Pregnancy and serum C.P.K. levels in potential carriers of severe X-linked muscular dystrophy.
    Lancet. 1971 Apr 24;1(7704):855-6 PMID: 4102542
  5. The effects of genetic counselling in Duchenne muscular dystrophy.
    Clin Genet. 1972;3(2):147-50 PMID: 5054316
Article Info
Journal
British medical journal
Abbr.
Br Med J
ISSN
0007-1447
Published
1976-09-04
Pages
577-9
Language
English
Region
England
NLM ID
0372673
PMCID
PMC1688064
Subset
IM
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