A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes
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...
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Palacký University Olomouc, Faculty of Medicine and Dentistry
2016-06-01
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doaj-a534bd9e0d49468296125c2fdeb79d622020-11-25T03:33:43ZengPalacký University Olomouc, Faculty of Medicine and DentistryBiomedical Papers1213-81181804-75212016-06-01160231031510.5507/bp.2016.020bio-201602-0020A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis SyndromesOle Jung0Ralf Smeets1Henning Hanken2Reinhard E. Friedrich3Max Heiland4Amir Tagniha5Brian Labow6Department of Plastic and Oral Surgery, Children´s Hospital Boston, Harvard Medical School, Boston, USADepartment of Oral and Maxillofacial Surgery, University Medical Center Hamburg, Hamburg, GermanyDepartment of Oral and Maxillofacial Surgery, University Medical Center Hamburg, Hamburg, GermanyDepartment of Oral and Maxillofacial Surgery, University Medical Center Hamburg, Hamburg, GermanyDepartment of Oral and Maxillofacial Surgery, University Medical Center Hamburg, Hamburg, GermanyDepartment of Plastic and Oral Surgery, Children´s Hospital Boston, Harvard Medical School, Boston, USADepartment of Plastic and Oral Surgery, Children´s Hospital Boston, Harvard Medical School, Boston, USAAim: 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.https://biomed.papers.upol.cz/artkey/bio-201602-0020_A_patient_with_Charlie_M_Syndrome_Differential_diagnosis_of_Oromandibular_Limb_Hypogenesis_Syndromes.phporomandibular limb hypogenesis syndromes (olhs)charlie m syndromeoromandibular and limb hypogenesis malformations (olhm) |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ole Jung Ralf Smeets Henning Hanken Reinhard E. Friedrich Max Heiland Amir Tagniha Brian Labow |
spellingShingle |
Ole Jung Ralf Smeets Henning Hanken Reinhard E. Friedrich Max Heiland Amir Tagniha Brian Labow A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes Biomedical Papers oromandibular limb hypogenesis syndromes (olhs) charlie m syndrome oromandibular and limb hypogenesis malformations (olhm) |
author_facet |
Ole Jung Ralf Smeets Henning Hanken Reinhard E. Friedrich Max Heiland Amir Tagniha Brian Labow |
author_sort |
Ole Jung |
title |
A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes |
title_short |
A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes |
title_full |
A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes |
title_fullStr |
A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes |
title_full_unstemmed |
A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes |
title_sort |
patient with charlie m syndrome: differential diagnosis of oromandibular limb hypogenesis syndromes |
publisher |
Palacký University Olomouc, Faculty of Medicine and Dentistry |
series |
Biomedical Papers |
issn |
1213-8118 1804-7521 |
publishDate |
2016-06-01 |
description |
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. |
topic |
oromandibular limb hypogenesis syndromes (olhs) charlie m syndrome oromandibular and limb hypogenesis malformations (olhm) |
url |
https://biomed.papers.upol.cz/artkey/bio-201602-0020_A_patient_with_Charlie_M_Syndrome_Differential_diagnosis_of_Oromandibular_Limb_Hypogenesis_Syndromes.php |
work_keys_str_mv |
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