Familial cerebellar ataxia and hypogonadism associated with sensorimotor axonal polyneuropathy

In this article, we report two siblings who have familial cerebellar ataxia and hypogonadism associated with sensorimotor axonal polyneuropathy documented by light microscopy. This combination has not been reported previously in the literature. Cerebellar ataxia and hypogonadism is reviewed accordin...

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Veröffentlicht in:	Clinical neurology and neurosurgery 2000-09, Vol.102 (3), p.129-134
Hauptverfasser:	ERDEMOGLU, A. Kemal, AKBOSTANCI, M. Cenk, SELCUKI, Deniz
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Atrophy Biological and medical sciences Cerebellar ataxia Cerebellar Ataxia - blood Cerebellar Ataxia - genetics Cerebellar Ataxia - pathology Cerebellum - diagnostic imaging Cerebellum - pathology Consanguinity Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Gonadotropins, Pituitary - blood Hereditary Sensory and Motor Neuropathy - blood Hereditary Sensory and Motor Neuropathy - complications Hereditary Sensory and Motor Neuropathy - genetics Hereditary Sensory and Motor Neuropathy - pathology Histopathology Humans Hypogonadism Hypogonadism - blood Hypogonadism - genetics Hypogonadism - pathology Male Medical sciences Neurology Pedigree Polyneuropathy Sural Nerve - pathology Syndrome Testosterone - blood Tomography, X-Ray Computed Tropical medicine
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Zusammenfassung:	In this article, we report two siblings who have familial cerebellar ataxia and hypogonadism associated with sensorimotor axonal polyneuropathy documented by light microscopy. This combination has not been reported previously in the literature. Cerebellar ataxia and hypogonadism is reviewed according to the clinical and laboratory features of the reported cases in the literature.
ISSN:	0303-8467 1872-6968
DOI:	10.1016/S0303-8467(00)00077-9