Publication:
McCune Albright Syndrome: A Case Report

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorKarki, Subhana Thapa
dc.contributor.authorJain, Vandana
dc.date.accessioned2026-01-01T06:45:58Z
dc.date.available2026-01-01T06:45:58Z
dc.date.issued2020
dc.descriptionSubhana Thapa Karki Department of Paediatrics, Kanti Children’s Hospital, Maharajgunj, Kathmandu, Nepal Vandana Jain Department of Paediatrics, All India Institute of Medical Sciences, New Delhi, India
dc.description.abstractAbstract: McCune Albright syndrome (MAS) is a very rare genetic disease characterised by any two of the following three findings: café au lait spots, polyosteotic fibrous dysplasia and endocrine disorders. The clinical presentation of MAS may vary depending on which of the various components of the syndrome predominate. Here, we report one case of MAS presenting with precocious puberty.
dc.identifierhttps://doi.org/10.3126/jnps.v40i2.29099
dc.identifier.urihttps://hdl.handle.net/20.500.14572/3967
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectCafé au lait spots
dc.subjectMcCune-Albright syndrome
dc.subjectPolyosteotic fibrous dysplasia
dc.subjectPrecocious puberty
dc.titleMcCune Albright Syndrome: A Case Report
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage137
oaire.citation.startPage134
relation.isJournalIssueOfPublication2824c45f-d40b-4646-b754-b63604ec415f
relation.isJournalIssueOfPublication.latestForDiscovery2824c45f-d40b-4646-b754-b63604ec415f
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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