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A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes

O. Jung, R. Smeets, H. Hanken, R. E. Friedrich, M. Heiland, A. Tagniha, B. Labow

. 2016 ; 160 (2) : 310-315. [pub] 20160427

Jazyk angličtina Země Česko

Typ dokumentu kazuistiky, časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc17012969

AIM: In order to provide adequate treatment to a patient with a subtype of Oromandibular Limb Hypogenesis Syndromes (OLHS), this study aimed to review and to analyze the current literature and treatment options of OLHS. METHODS: Literature review in PubMed and Sciencedirect. Due to the small number of results, all available references were analyzed precisely. RESULTS: Cases of OLHS are formerly rare and often incomplete. There are various classifications available, which, however, often seem confusing and are of little practical relevance. Furthermore, we present a complete case report of a patient with Charlie M syndrome, a type IV (Chicarilli)/ V (Hall) OLHS malformation. We also describe embryologic pathogenesis and differential diagnoses. CONCLUSION: As a result of our literature review, we recommend an adjusted classification for OLHS.

Citace poskytuje Crossref.org

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