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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
Language English Country Czech Republic
Document type Case Reports, Journal Article
NLK
Directory of Open Access Journals
from 2001
Free Medical Journals
from 1998
Medline Complete (EBSCOhost)
from 2007-06-01
ROAD: Directory of Open Access Scholarly Resources
from 2001
PubMed
27132808
DOI
10.5507/bp.2016.020
Knihovny.cz E-resources
- MeSH
- Diagnosis, Differential MeSH
- Craniofacial Abnormalities diagnosis surgery MeSH
- Humans MeSH
- Mandible abnormalities MeSH
- Intellectual Disability diagnosis surgery MeSH
- Young Adult MeSH
- Abnormalities, Multiple diagnosis surgery MeSH
- Retinitis Pigmentosa diagnosis surgery MeSH
- Foot Deformities, Congenital diagnosis MeSH
- Check Tag
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
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.
Department of Oral and Maxillofacial Surgery University Medical Center Hamburg Hamburg Germany
Department of Plastic and Oral Surgery Children´s Hospital Boston Harvard Medical School Boston USA
References provided by Crossref.org
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- $a 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.
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