𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Metachromatic leukodystrophy: On an atypical case

✍ Scribed by C. A. Zambrino; U. Balottin; A. Minelli; G. Rossi; G. Lanzi


Publisher
Springer Milan
Year
1992
Tongue
English
Weight
221 KB
Volume
13
Category
Article
ISSN
1590-1874

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Atypical metachromatic leukodystrophy?
✍ T. TΓΈnnesen; C. Vrang; U. N. Wiesmann; H. Christomanou; H. O. Lou πŸ“‚ Article πŸ“… 1984 πŸ› Springer 🌐 English βš– 410 KB

A 3 1/2-year-old slightly retarded boy with marked deficiency of arylsulfatase A (ASA) activity in leucocytes and fibroblasts and almost no cerebroside sulfatase (CS) activity in fibroblasts was tested with the sulfatide-loading test. On this test his fibroblasts showed impaired degradation. A patho

Atypical clinical course in juvenile met
✍ Banu Anlar; John S Waye; Barry Eng; Kader Karli πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 648 KB

A male and female with juvenile metachromatic leukodystrophy (MLD) with unusual manifestations are presented, each involving a novel arylsulfatase A gene mutation. One patient demonstrated acute intermittent encephalopathic episodes for 1 year after having received the diagnosis of MLD at the age of

Late-onset metachromatic leukodystrophy:
✍ D. Seidel; H. H. Goebel; W. Scholz πŸ“‚ Article πŸ“… 1981 πŸ› Springer 🌐 English βš– 961 KB

A 20-year-old female had psychiatric symptoms of organic brain disease for five years but without clinical or neurophysiological signs of polyneuropathy. Late-onset metachromatic leukodystrophy was confirmed by finding severely reduced arylsulfatase A activity in her urine and leukocytes, marked exc