Humoral immunodeficiency in congenital insensitivity to pain with anhidrosis

Neurogenetics

Volumn 10, Issue 2, 2009, Pages 161-165

  Kilic, Sara Sebnem ^a   Ozturk, Rifatcan ^a   Sarisozen, Bartu ^a   Rotthier, Annelies ^b   Baets, Jonathan ^b   Timmerman, Vincent ^b  

^a ULUDAG UNIVERSITY   (Turkey)

^b UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

Hereditary sensory and autonomic neuropathy; Hip dislocation; Hypogammaglobulinemia; Immunodeficiency; Insensitivity to pain

Indexed keywords

IMMUNOGLOBULIN;

ANHIDROSIS; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; AVASCULAR NECROSIS; BRACE; CASE REPORT; CAST APPLICATION; CHILD; CLINICAL FEATURE; CONGENITAL ANALGESIA; CONGENITAL INSENSITIVITY TO PAIN WITH ANHIDROSIS; DISEASE ASSOCIATION; FEMALE; GENE; GENE DELETION; GENE SEQUENCE; HIP DISLOCATION; HUMAN; IMMUNOGLOBULIN DEFICIENCY; NTRK1 GENE; PRIORITY JOURNAL; RECURRENT DISEASE; RECURRENT INFECTION; SCHOOL CHILD; SEQUENCE ANALYSIS;

CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; HYPOHIDROSIS; IMMUNOGLOBULINS, INTRAVENOUS; IMMUNOLOGIC DEFICIENCY SYNDROMES; PAIN INSENSITIVITY, CONGENITAL; PHENOTYPE; RECEPTOR, TRKA;

EID: 64149117822     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10048-008-0165-x     Document Type: Article

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