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Congenital hypomyelinating neuropathy.
Indian Pediatr ; 2003 Nov; 40(11): 1084-7
Article in English | IMSEAR | ID: sea-11584
ABSTRACT
An eleven-month-old baby born out of non-consanguineous parentage presented with history of delayed motor milestones. The weakness was predominantly distal; there was intercostal muscle weakness, generalized hypotonia and areflexia. The nerve conduction velocities were unobtainable in all the four limbs. Sural nerve biopsy was consistent with the diagnosis of congenital hypomyelinating neuropathy, a rare form of hereditary motosensory neuropathy.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Prognosis / Biopsy, Needle / Severity of Illness Index / Female / Humans / Prednisolone / Immunohistochemistry / Hereditary Sensory and Motor Neuropathy / Physical Therapy Modalities / Treatment Outcome Type of study: Prognostic study Country/Region as subject: Asia Language: English Journal: Indian Pediatr Year: 2003 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Prognosis / Biopsy, Needle / Severity of Illness Index / Female / Humans / Prednisolone / Immunohistochemistry / Hereditary Sensory and Motor Neuropathy / Physical Therapy Modalities / Treatment Outcome Type of study: Prognostic study Country/Region as subject: Asia Language: English Journal: Indian Pediatr Year: 2003 Type: Article