Literature DB >> 2854735

Familial dysautonomia manifesting as neonatal nemaline myopathy.

N Amir1, J Chemke, Y Shapira.   

Abstract

An infant presented with congenital hypotonia, poor sucking, apathy, and areflexia. Muscle biopsy at two months of age revealed numerous nemaline rods, suggesting congenital nemaline myopathy. During the ensuing months, familial dysautonomia was suggested by recurrent pulmonary infections, dysphagia, alacrima, hyperhydrosis, emotional lability, and unexplained episodes of hyperthermia and breath-holding spells. The diagnosis was confirmed by positive intradermal histamine and ocular mecholyl tests. The finding of nemaline rods adds a new facet to the recognized polymorphic presentation of familial dysautonomia.

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Year:  1985        PMID: 2854735     DOI: 10.1016/s0887-8994(85)80011-4

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  2 in total

1.  Follow-up studies in a case of unusual congenital myopathy, suggestive of nemaline type.

Authors:  E Gibbels; K Kellermann; H J Schädlich; R Adams; W F Haupt
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

2.  Increased frequency of rhabdomyolysis in familial dysautonomia.

Authors:  Jose-Alberto Palma; Ricardo Roda; Lucy Norcliffe-Kaufmann; Horacio Kaufmann
Journal:  Muscle Nerve       Date:  2015-08-13       Impact factor: 3.217

  2 in total

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