Publication: A ‘Missed’ Diagnosed Case of Christ-Siemens-Touraine Syndrome
Date
2017
Authors
Article Type
Case Report
Journal Title
Journal ISSN
ISSN 1990-7974 eISSN 1990-7982
Volume Title
Pages
Pages: 83 - 85
Publisher
Nepal Paediatric Society (JNPS)
Abstract
Abstract:
Christ-Siemens-Touraine syndrome also known as Anhidrotic ectodermal dysplasia, is a rare genetic disorder, occurring in 1-100,000 live male births. A two year old male child with classical signs and symptoms of the disease, affecting skin, hairs, nails and teeth, misdiagnosed initially as a case of seborrhic dermatitis, and later as tuberculosis, is described here. Treatment includes counselling the family, skin care, avoiding high ambient temperature, and prosthodontic measures. Diagnosis as early as possible, based mainly on clinical features can prevent mortality due to hyperpyrexia and respiratory infections. Beyond early childhood, life expectancy is normal to slightly reduced.
Description
Shambhavi Narayan
S.M.S. Medical College, Jaipur, Rajasthan
Keywords
hyperthermia, alopecia
Identifier
https://doi.org/10.3126/jnps.v37i1.16247