Literature DB >> 18657423

Expanded HSAN4 phenotype associated with two novel mutations in NTRK1.

Stefan Wieczorek1, Jonas Bergström, Maria Sääf, Judith Kötting, Erik Iwarsson.   

Abstract

Hereditary sensory and autonomic neuropathy type IV (HSAN4) is a severe autosomal recessive disorder characterized by childhood onset of sensory and autonomic dysfunction leading to hyperthermia, recurrent infections and physical impairment due to complications of osteoarthritis. Cognitive impairment and aggressive behaviour is common. HSAN4 is caused by mutations in the NTRK1 gene coding for the tyrosine kinase receptor A. We present detailed description of a rare, mild HSAN4 phenotype associated with two novel NTRK1 mutations. This Swedish patient presents with an adult onset of painful Charcot arthropathy, prolonged wound healing, discrete polyneuropathy, hypohidrosis without further autonomic dysfunction and no cognitive affection.

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Year:  2008        PMID: 18657423     DOI: 10.1016/j.nmd.2008.06.370

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  2 in total

Review 1.  Mechanisms of disease in hereditary sensory and autonomic neuropathies.

Authors:  Annelies Rotthier; Jonathan Baets; Vincent Timmerman; Katrien Janssens
Journal:  Nat Rev Neurol       Date:  2012-01-24       Impact factor: 42.937

Review 2.  Phenotypic heterogeneity of intellectual disability in patients with congenital insensitivity to pain with anhidrosis: A case report and literature review.

Authors:  Zhenlei Liu; Jiaqi Liu; Gang Liu; Wenjian Cao; Sen Liu; Yixin Chen; Yuzhi Zuo; Weisheng Chen; Jun Chen; Yu Zhang; Shishu Huang; Guixing Qiu; Philip F Giampietro; Feng Zhang; Zhihong Wu; Nan Wu
Journal:  J Int Med Res       Date:  2018-04-05       Impact factor: 1.671

  2 in total

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