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PMID: 485196 Published · ppublish English Journal Article

Carrier detection in Duchenne muscular dystrophy. Evidence from a study of obligatory carriers and mothers of isolated cases.

Archives of disease in childhood ·Vol. 54 ·No. 7 ·1979-07-00 ·Pages 534-7

Sibert JR, Harper PS, Thompson RJ, Newcombe RG

Abstract

The mean levels of serum creatinine phosphokinase (CPK) were studied in three groups of women: normal controls (57), obligate carriers for Duchenne muscular dystrophy (30), and mothers of isolated cases of this disease (35). The distribution of the levels in these groups was significantly different and was in keeping with the hypothesis that one-third of isolated cases result from new mutations. The control and carrier ranges overlapped considerably, with the level of CPK of 33% of obligate carriers coming within the 97 1/2 centile of the normal range. Odds against an individual being a carrier were derived for specific mean values of CPK. They should be considered with genetic information using Bayes's theorem. The mean CPK levels in obligate carriers showed significant familial clustering. This may have implications in carrier detection.

MeSH Terms
Clinical Enzyme Tests Creatine Kinase/blood Female Genetic Carrier Screening Humans Muscular Dystrophies/diagnosis,genetics,prevention & control Probability
Chemicals
Creatine Kinase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Sibert J R
Harper P S
Thompson R J
Newcombe R G
References (8)
8 references, click to expand
  1. 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
  2. An assessment of the creatine kinase test in the detection of carriers of Duchenne muscular dystrophy.
    J Pediatr. 1967 Jul;71(1):82-93 PMID: 5293863
  3. Systemic membrane defect in the proximal muscular dystrophies.
    N Engl J Med. 1978 Oct 19;299(16):841-6 PMID: 308614
  4. Use of creatine kinase for detecting severe X-linked muscular dystrophy carriers.
    Br Med J. 1976 Sep 4;2(6035):577-9 PMID: 963439
  5. Genetic counselling in X-linked muscular dystrophy.
    J Neurol Sci. 1969 May-Jun;8(3):579-87 PMID: 4185251
  6. The detection of carriers of X-linked muscular dystrophy genes. A review of some methods studied in Newcastle upon Tyne.
    J Neurol Sci. 1971 Aug;13(4):459-74 PMID: 5570764
  7. The biochemical identification of the carrier state in X-linked recessive (Duchenne) muscular dystrophy.
    Clin Chim Acta. 1969 Nov;26(2):207-21 PMID: 5352692
  8. Carrier detection in Duchenne muscular dystrophy.
    N Engl J Med. 1976 Jan 22;294(4):193-8 PMID: 1244534
Article Info
Journal
Archives of disease in childhood
Abbr.
Arch Dis Child
ISSN
1468-2044
Published
1979-07-00
Pages
534-7
Language
English
Region
England
NLM ID
0372434
PMCID
PMC1545480
Subset
IM
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