A case of a hereditary, late progressing sensory autonomic neuropathy

Clinical Neuropathology

Volumn 17, Issue 1, 1998, Pages 12-14

  Cinar, Y ^a,c   Hekimoglu F ^a   Ince, B ^b   Ince, U ^a   Onganer, E ^a  

^a HAYDARPASA NUMUNE HOSPITAL   (Turkey)

^b ISTANBUL UNIVERSITY   (Turkey)

^c NONE   (Turkey)

Author keywords

Hereditary sensory autonomic neuropathy

Indexed keywords

ADULT; ARTICLE; AUTONOMIC NEUROPATHY; CASE REPORT; DISEASE CLASSIFICATION; FEMALE; HUMAN; PRIORITY JOURNAL; SENSORY NERVE; TENDON REFLEX;

ADULT; COMBINED MODALITY THERAPY; DISEASE PROGRESSION; FEMALE; HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; HUMANS;

EID: 0031940417     PISSN: 07225091     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

1. Axelrod FB, Iyer K, Fish I et al 1981 Progressive sensory loss in familial dysautonomia. Paediatrics 67: 517
2. Blumenfeld A, Slaugenhaupt SA, Axelrod FB et al 1993 Localisation of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis. Nat Genet 4: 160-164
3. Daman MJ, Carpenter S 1985 Hereditary sensory neuropathy: Biopsy study of an autosomal dominant study. Neurology 35: 1226-1229
4. Dyck PJ 1993 Neuronal atrophy and degeneration predominantly affecting peripheral sensory and autonomic neurons. In: Dyck PJ, Thomas PK, Griffin JW, Low PA, Podutb JF (eds) Peripheral Neuropathy. 3rd edn. Saunders, Philadelphia, pp 1065-1093
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