A new N-acetyl-beta-D-hexosaminidase disease with late onset of progressive neurological symptoms
Författare
Summary, in English
Clinical data are presented on a 30-year-old male with normal early development (4-5 years) but subsequent progressive impairment of psychomotor functions. He has marked kyphoscoliosis and talipes calcaneo-valgus. The organs appear normal and the patient can walk unaided and feed himself although he does not recognize his parents. He has normal fundi oculi. Biochemical data show an absence of mucopolysacchariduria and very low but detectable levels of N-acetyl-beta-D-hexosaminidase in serum and leucocytes. The clinical symptoms are much milder than would normally be expected from such a profound enzyme deficiency (Sandhoff disease).
Avdelning/ar
Publiceringsår
1979
Språk
Engelska
Sidor
124-128
Publikation/Tidskrift/Serie
Human Heredity
Volym
29
Issue
2
Dokumenttyp
Artikel i tidskrift
Förlag
Karger
Ämne
- Medical Genetics
Status
Published
ISBN/ISSN/Övrigt
- ISSN: 1423-0062