Breast reconstruction in a patient with Noonan syndrome

Noonan syndrome (NS) is a relatively common genetic disorder with an autosomal dominant inheritance pattern affecting 1 in 1000–2500 births. Patients with this syndrome present with characteristic facial, musculoskeletal, cardiac and endocrine abnormalities. Lack of postpubertal breast development i...

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Vydáno v:BMJ Case Rep
Hlavní autoři: Sharaf, Basel, Sabbagh, Mohamed Diya, Roh, Si-Gyun
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Publishing Group 2017
Témata:
Novel Treatment (New Drug/Intervention; Established Drug/Procedure in New Situation)
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5695322/
https://ncbi.nlm.nih.gov/pubmed/29092974
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2017-222325
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