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Kenny-Caffey syndrome type 1 in an Egyptian girl

Kenny-Caffey syndrome type 1 (KCS1) (OMIM 244460) is a rare syndrome characterized by growth retardation, uniformly small slender long bones with medullary stenosis, thickened cortex of the long bones, hypocalcemia possibly with tetany at an early age and normal intelligence. The primary outcome of...

詳細記述

保存先:
書誌詳細
主要な著者: Metwalley, Kotb Abbass, Farghaly, Hekma Saad
フォーマット: Artigo
言語:Inglês
出版事項: Medknow Publications & Media Pvt Ltd 2012
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3475915/
https://ncbi.nlm.nih.gov/pubmed/23087875
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2230-8210.100645
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