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Acute flaccid paraparesis (cauda equina syndrome) in a patient with Bardet–Biedl syndrome

Bardet–Biedl syndrome (BBS) is a rare, autosomal-recessive, debilitating genetic disorder, which can present with multitudinous systemic clinical features including rod-cone dystrophy, polydactyly, Frohlich-like central obesity, mental retardation, hypogonadism, and renal anomalies. Diverse neuromus...

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Bibliografische gegevens
Gepubliceerd in:Indian J Orthop
Hoofdauteurs: Viswanathan, Vibhu Krishnan, Kanna, Rishi Mugesh, Shetty, Ajoy Prasad, Rajasekaran, S
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Medknow Publications & Media Pvt Ltd 2017
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5439321/
https://ncbi.nlm.nih.gov/pubmed/28566787
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0019-5413.205682
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