Alstrom - A rare condition associated with diabetes;Alstrom-syndrom - Eine seltene Erkrankung aus dem diabetischen Formenkreis

Medizinische Klinik

Volumn 92, Issue 3, 1997, Pages 175-178

  Weichenhain, Brigitte ^a   Stemplinger, Johannes ^b   Ziegler, Anette Gabriele ^b   Rabl, Wolfgang ^c   Standl, Eberhard ^b   Stiegler, Hubert ^a  

^a Angiologische Abteilung   (Germany)

^b Stadtischen Krankhs Munchen S   (Germany)

^c TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; HUMAN; HYPOGONADISM; KIDNEY DISEASE; MALE; NON INSULIN DEPENDENT DIABETES MELLITUS; OBESITY; RETINITIS PIGMENTOSA; DIABETES MELLITUS; DIFFERENTIAL DIAGNOSIS; GENETICS; NUCLEOTIDE SEQUENCE; OPTIC NERVE ATROPHY; SECOND MESSENGER; SYNDROME;

BUNAZOSIN; QUINAZOLINE DERIVATIVE;

ADULT; DIABETES MELLITUS; DIABETES MELLITUS, TYPE 2; DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; HUMANS; MALE; OBESITY; OPTIC ATROPHY; QUINAZOLINES; RETINITIS PIGMENTOSA; SECOND MESSENGER SYSTEMS; SYNDROME;

EID: 0030892676     PISSN: 07235003     EISSN: None     Source Type: Journal    
DOI: 10.1007/bf03043276     Document Type: Article

References (9)

1. Alström, C. H., B. Hallgren, L. B. Nilsson, H. Asander; Retinal degeneration combined with obesity, diabetes mellitus and neurogenous deafness: a specific syndrome (not hitherto described) distinct from the Laurence-Moon-Bardet-Biedl syndrome. Acta psychiat. neurol. scand. 34, Suppl. 129 (1959), 1.
2. Edwards, J. A., P. K. Sethi, A. J. Scoma, R. M Bannerman, L. A. Frohman: A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance. Amer. J. Med. 60 (1976), 23-32.
3. Goldstein, J. L., P. J. Fialkow: The Alström syndrome. Medicine 52 (1973), 53-71.
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6. Pilz, D., O. W. Qurrell, E. W. Jones: Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD). J. med. Genet. 31 (1994), 328-330.
7. Reaven, G. M.: Role of insulin resistance in human disease. Diabetes 37 (1988), 1595-1607.
8. Standl, E., H. U. Janka, H. Stiegler, H. Mehnert: Hyper-insulinaemia and macrovascular complications in non-insulin-dependent diabetes mellitus. In: Lefèbvre, P. J., E. Standl (eds ): New aspects in diabetes. De Gruyter, Stuttgart - New York 1992, p. 87-95
9. Weinstein, R. L., B. Kliman, R. E. Scully: Familial syndrome of primary testicular insufficiency with normal virilization, blindness, deafness and metabolic abnormalities. New Engl. J. Med. 281 (1969), 969-977.