Multicore myopathy in a patient with anhidrotic ectodermal dysplasia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Anesthesiology and Pain Medicine,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF03008347.pdf
Reference17 articles.
1. Walpole IR, Goldblatt J. Rapp-Hodgkin hypohidrotic ectodermal dysplasia syndrome. Clin Genet 1991; 39: 114–20.
2. Sybert VP. Hypohidrotic ectodermal dysplasia: argument against an autosomal recessive form clinically indistinguishable from X-linked hypohidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome). Pediatr Dermatol 1989; 6: 76–81.
3. Siegel MB, Potsic WP. Ectodermal dysplasia: the otolaryngologic manifestations and management. Int J Pediatr Otorhinolaryngol 1990; 19: 265–71.
4. Clarke A, Phillips DI, Brown R, Harper PS. Clinical aspects of X-linked hypohidrotic ectodermal dysplasia. Arch-Dis-Child 1987; 62: 989–96.
5. Potter FC, Bowie MD. Dysphagia in hypohidrotic ectodermal dysplasia. A case report. S Afr Med J 1984; 66: 232–4.
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