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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...

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Bibliografiske detaljer
Main Authors: Metwalley, Kotb Abbass, Farghaly, Hekma Saad
Format: Artigo
Sprog:Inglês
Udgivet: Medknow Publications & Media Pvt Ltd 2012
Fag:
Online adgang: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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