Publication:
A ‘Missed’ Diagnosed Case of Christ-Siemens-Touraine Syndrome

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorNarayan, Shambhavi
dc.date.accessioned2026-02-09T06:57:19Z
dc.date.available2026-02-09T06:57:19Z
dc.date.issued2017
dc.descriptionShambhavi Narayan S.M.S. Medical College, Jaipur, Rajasthan
dc.description.abstractAbstract: 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.
dc.identifierhttps://doi.org/10.3126/jnps.v37i1.16247
dc.identifier.urihttps://hdl.handle.net/20.500.14572/4592
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjecthyperthermia
dc.subjectalopecia
dc.titleA ‘Missed’ Diagnosed Case of Christ-Siemens-Touraine Syndrome
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage85
oaire.citation.startPage83
relation.isJournalIssueOfPublication746230eb-c5af-4ac2-aa4b-ea6e90b44c32
relation.isJournalIssueOfPublication.latestForDiscovery746230eb-c5af-4ac2-aa4b-ea6e90b44c32
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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