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

Standard

A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes. / Jung, Ole; Smeets, Ralf; Hanken, Henning; Friedrich, Reinhard E; Heiland, Max; Tagniha, Amir; Labow, Brian.

in: BIOMED PAP, Jahrgang 160, Nr. 2, 06.2016, S. 310-5.

Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung

Harvard

Jung, O, Smeets, R, Hanken, H, Friedrich, RE, Heiland, M, Tagniha, A & Labow, B 2016, 'A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes', BIOMED PAP, Jg. 160, Nr. 2, S. 310-5. https://doi.org/10.5507/bp.2016.020

APA

Jung, O., Smeets, R., Hanken, H., Friedrich, R. E., Heiland, M., Tagniha, A., & Labow, B. (2016). A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes. BIOMED PAP, 160(2), 310-5. https://doi.org/10.5507/bp.2016.020

Vancouver

Jung O, Smeets R, Hanken H, Friedrich RE, Heiland M, Tagniha A et al. A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes. BIOMED PAP. 2016 Jun;160(2):310-5. https://doi.org/10.5507/bp.2016.020

Bibtex

@article{8222fc0d7f8d4f5ebb55c838dfc7f82b,
title = "A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes",
abstract = "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.",
author = "Ole Jung and Ralf Smeets and Henning Hanken and Friedrich, {Reinhard E} and Max Heiland and Amir Tagniha and Brian Labow",
year = "2016",
month = jun,
doi = "10.5507/bp.2016.020",
language = "English",
volume = "160",
pages = "310--5",
journal = "BIOMED PAP",
issn = "1213-8118",
publisher = "Palacky University",
number = "2",

}

RIS

TY - JOUR

T1 - A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes

AU - Jung, Ole

AU - Smeets, Ralf

AU - Hanken, Henning

AU - Friedrich, Reinhard E

AU - Heiland, Max

AU - Tagniha, Amir

AU - Labow, Brian

PY - 2016/6

Y1 - 2016/6

N2 - 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.

AB - 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.

U2 - 10.5507/bp.2016.020

DO - 10.5507/bp.2016.020

M3 - SCORING: Journal article

C2 - 27132808

VL - 160

SP - 310

EP - 315

JO - BIOMED PAP

JF - BIOMED PAP

SN - 1213-8118

IS - 2

ER -