Publication:
Hypohiderotic ectodermal dysplasia

creativeworkseries.issn1812-2027
dc.contributor.authorA, Neopane
dc.contributor.authorSK, Singh
dc.contributor.authorB, Manandhar
dc.date.accessioned2025-07-24T07:48:24Z
dc.date.available2025-07-24T07:48:24Z
dc.date.issued2006
dc.descriptionNeopane A 1, Singh SK 2 , Manandhar B3 1 Assistant Professor in Paediatrics (NAMS), 2Assistant Professor in Pathology (NAMS), Shree Birendra Hospital, Chhauni, 3 Resident in Paediatrics, National Academy of Medical Sciences, Bir Hospital
dc.description.abstractWe report a case of a six years age girl who presented to our out patients department with the history and findings suggestive of recurrent respiratory tract infections. She was also noticed to have; non homogeneous hyper- pigmented patches on the face since three months of age, sparse hair on the scalp and eyebrows, conical peg like teeth and delayed dentition, prominent and low set ears, perpetually flexed third toe bilaterally. Axillary skin biopsy showed adenexal structures and eccrine glands in subcutaneous fat which were reduced in number. The diagnosis made was: Anhydrotic/ Hypohidrotic type of ectodermal dysplasia. Key words: Ectodermal Dysplasia, Anhidreotic, Hypohidrotic
dc.identifier.urihttps://hdl.handle.net/20.500.14572/604
dc.language.isoen_US
dc.publisherKathmandu University
dc.titleHypohiderotic ectodermal dysplasia
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage521
oaire.citation.startPage520
relation.isJournalIssueOfPublication33ef012a-4a08-47e9-beb2-7862118d90bf
relation.isJournalIssueOfPublication.latestForDiscovery33ef012a-4a08-47e9-beb2-7862118d90bf
relation.isJournalOfPublicationa782b7ff-cf89-4178-ad1c-11ed89cfe1bd

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