𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Myoadenylate deaminase deficiency with severe rhabdomyolysis

✍ Scribed by F. A. M. Baumeister; M. Gross; D. R. Wagner; D. Pongratz; R. Eife

Book ID
105411769
Publisher
Springer
Year
1993
Tongue
English
Weight
420 KB
Volume
152
Category
Article
ISSN
0340-6997

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Type 2a fibre rhabdomyolysis in myoadeny
Type 2a fibre rhabdomyolysis in myoadenylate deaminase deficiency
✍ C. Zimmer; H. Altenkirch; S. DorfmΓΌller-KΓΌchlin; D. Pongratz; I. Paetzke; G. Gos πŸ“‚ Article πŸ“… 1991 πŸ› Springer 🌐 English βš– 614 KB

A 31-year-old woman developed an acute, potentially fatal rhabdomyolysis of undetermined origin. Muscle biopsy revealed selective lysis involving exclusively type 2a fibers. Myoadenylate-deaminase (MAD) deficiency was proven by a negative histochemical reaction as well as by an enzymatic biochemical

Myoadenylate deaminase deficiency
Myoadenylate deaminase deficiency
✍ Dr. Jack B. Shumate; Dr. Richard Katnik; Martha Ruiz Ms; Kenneth Kaiser Mr; Dr. πŸ“‚ Article πŸ“… 1979 πŸ› John Wiley and Sons 🌐 English βš– 385 KB
Genetic characteristics of myoadenylate
Genetic characteristics of myoadenylate deaminase deficiency
✍ H. T. F. M. Verzijl; Dr. B. G. M. van Engelen; J. A. F. M. Luyten; G. C. H. Stee πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 663 KB

Two types of myoadenylate deaminase (MAD) deficiency have been described, primary or inherited, and secondary or acquired MAD deficiency. In this study, we investigated whether secondary MAD deficiency is indeed acquired or merely coincidental. We demonstrated the same underlying molecular defect, a