Fetal plasma carbonic anhydrase III in prenatal diagnosis of duchenne muscular dystrophy

1985 ◽  
Vol 20 (1) ◽  
pp. 115-122 ◽  
Author(s):  
Robert Heath ◽  
Nicholas D. Carter ◽  
Stephen Jeffery ◽  
Robert J. Edwards ◽  
David C. Watts ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Duchenne Muscular Dystrophy ◽  
Muscular Dystrophy ◽  
Carbonic Anhydrase ◽  
Fetal Plasma ◽  
Carbonic Anhydrase Iii

Carbonic anhydrase III in Duchenne muscular dystrophy

1983 ◽  
Vol 133 (2) ◽  
pp. 201-208 ◽  
Author(s):  
N.D. Carter ◽  
R. Heath ◽  
S. Jeffery ◽  
M.J. Jackson ◽  
D.J. Newham ◽  
...  
Keyword(s):  
Duchenne Muscular Dystrophy ◽  
Muscular Dystrophy ◽  
Carbonic Anhydrase ◽  
Carbonic Anhydrase Iii

Carbonic anhydrase III in serum in muscular dystrophy and other neurological disorders: relationship with creatine kinase

1991 ◽  
Vol 37 (1) ◽  
pp. 36-39 ◽  
Author(s):  
Mitsuhlro Ohta ◽  
Yasuko Itagaki ◽  
Nobuyukl Itoh ◽  
Kyozo Hayashi ◽  
Hirosh Nishitani ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Creatine Kinase ◽  
Duchenne Muscular Dystrophy ◽  
Muscular Dystrophy ◽  
Carbonic Anhydrase ◽  
Neurological Disorders ◽  
Muscular Atrophy ◽  
Carbonic Anhydrase Iii ◽  
Severity Of The Disease ◽  
Lateral Sclerosis

Abstract We measured with a radioimmunoassay the concentrations of carbonic anhydrase III (CA-III, EC 4.2.1.1) in sera from 68 patients with muscular dystrophy, 10 carriers of Duchenne muscular dystrophy (DMD), and 63 patients with other neurological disorders. The values obtained were compared with those for creatine kinase (CK, EC 2.7.3.2). Serum CA-III was strikingly increased in patients with DMD (mean, 274.4 micrograms/L) and congenital (Fukuyama-type) (182.8 micrograms/L) and limb-girdle (203.7 micrograms/L) dystrophies and positively correlated with the activities of CK in patients with DMD. CA-III concentration decreased with the subjects' age and the severity of the disease, similar to the tendency observed between age or severity and the concentration of CK. We found moderately increased CA-III in patients with polymyositis, myotonic dystrophy, amyotrophic lateral sclerosis, spinal progressive muscular atrophy, or Kugelberg-Welander disease and in carriers of DMD.

Prenatal diagnosis of Duchenne muscular dystrophy by radio-immunoassay of myoglobin in amniotic fluid

2008 ◽  
Vol 21 (5) ◽  
pp. 354-355 ◽  
Author(s):  
O. Török ◽  
K. Norregaard-Hansen ◽  
M. Szokol ◽  
K. Csécsei ◽  
A. Harsányi ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Duchenne Muscular Dystrophy ◽  
Muscular Dystrophy ◽  
Amniotic Fluid ◽  
Radio Immunoassay

scholarly journals Assessment of 6 STR loci for prenatal diagnosis of Duchenne Muscular Dystrophy

2019 ◽  
Vol 58 (5) ◽  
pp. 645-649 ◽  
Author(s):  
Linh Thuy Dinh ◽  
Van Khanh Tran ◽  
Long Hoang Luong ◽  
Phuong Thi Le ◽  
Anh Duy Nguyen ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Duchenne Muscular Dystrophy ◽  
Muscular Dystrophy ◽  
Str Loci

Fetal Plasma Carbonic Anhydrase III and Creatine Kinase in Duchenne Dystrophy

1984 ◽  
Vol 429 (1 Biology and C) ◽  
pp. 620-622 ◽  
Author(s):  
R. HEATH ◽  
N. CARTER ◽  
S. JEFFERY ◽  
R. EDWARDS ◽  
D. WATTS ◽  
...  
Keyword(s):  
Creatine Kinase ◽  
Carbonic Anhydrase ◽  
Duchenne Dystrophy ◽  
Fetal Plasma ◽  
Carbonic Anhydrase Iii

scholarly journals POSSIBILITY OF PRENATAL DIAGNOSIS OF DUCHENNE MUSCULAR DYSTROPHY (DMD)

1977 ◽  
Vol 11 (4) ◽  
pp. 457-457 ◽  
Author(s):  
Florence P Haseltine ◽  
Maurice J Mahonev ◽  
John C Hobbins ◽  
C Thomas Caskey ◽  
Leon Roaenberg
Keyword(s):  
Prenatal Diagnosis ◽  
Duchenne Muscular Dystrophy ◽  
Muscular Dystrophy
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