A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes
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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, Vol. 160, No. 2, 06.2016, p. 310-5.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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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 -