Carrier detection in Duchenne muscular dystrophy.
Open Access
- 1 June 1980
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 17 (3) , 165-169
- https://doi.org/10.1136/jmg.17.3.165
Abstract
Serum creatine kinase, myoglobin, and percentage lymphocyte capping was determined in ten patients with Duchenne muscular dystrophy, 12 carriers (nine definite and three probable), 16 other female relatives, and eight normal controls. There was no detectable difference in lymphocyte capping ability between any of these clinical groups. Significant myoglobinaemia was present in all the affected males, but the difference in levels between carriers and controls suggested that this test has no advantage over creatine kinase estimations in carrier detection.This publication has 12 references indexed in Scilit:
- Serum creatine kinase levels in normal females.Journal of Medical Genetics, 1979
- Lymphocyte capping and carrier detection in Duchenne muscular dystrophy.BMJ, 1978
- Systemic Membrane Defect in the Proximal Muscular DystrophiesNew England Journal of Medicine, 1978
- Muscles, Membranes and Maternal MarkersNew England Journal of Medicine, 1978
- MYOGLOBINÆMIA IN DUCHENNE MUSCULAR DYSTROPHY PATIENTS AND CARRIERS: A NEW ADJUNCT TO CARRIER DETECTIONThe Lancet, 1978
- Diminished cap formation in lymphocytes from patients and carriers of Duchenne muscular dystrophy.Clinical Chemistry, 1977
- Distinctive Functional Properties of Human Blood L Lymphocytes: A Comparison with T Lymphocytes, B Lymphocytes, and MonocytesThe Journal of Immunology, 1977
- Electron spin resonance studies of erythrocyte membranes in muscular dystrophyAccounts of Chemical Research, 1977
- Duchenne dystrophyNeurology, 1975
- Erythrocyte Deformation in Human Muscular DystrophyScience, 1974