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Craniofacial disorders and dysplasias: Molecular, clinical, and management perspectives.

作者信息

Akintoye Sunday O, Adisa Akinyele O, Okwuosa Chukwubuzor U, Mupparapu Mel

机构信息

Department of Oral Medicine, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, United States of America.

University of Ibadan and University College Hospital Ibadan, Ibadan, Nigeria.

出版信息

Bone Rep. 2024 Mar 1;20:101747. doi: 10.1016/j.bonr.2024.101747. eCollection 2024 Mar.

DOI:10.1016/j.bonr.2024.101747
PMID:38566929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10985038/
Abstract

There is a wide spectrum of craniofacial bone disorders and dysplasias because embryological development of the craniofacial region is complex. Classification of craniofacial bone disorders and dysplasias is also complex because they exhibit complex clinical, pathological, and molecular heterogeneity. Most craniofacial disorders and dysplasias are rare but they present an array of phenotypes that functionally impact the orofacial complex. Management of craniofacial disorders is a multidisciplinary approach that involves the collaborative efforts of multiple professionals. This review provides an overview of the complexity of craniofacial disorders and dysplasias from molecular, clinical, and management perspectives.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e58/10985038/19847384fce9/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e58/10985038/bbe92b371eb1/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e58/10985038/ce7c9383d967/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e58/10985038/e87ed9ac96bd/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e58/10985038/19847384fce9/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e58/10985038/bbe92b371eb1/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e58/10985038/ce7c9383d967/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e58/10985038/e87ed9ac96bd/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e58/10985038/19847384fce9/gr4.jpg

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Craniofacial disorders and dysplasias: Molecular, clinical, and management perspectives.

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本文引用的文献

[1]
Dental anomalies in individuals with osteogenesis imperfecta: a systematic review and meta-analysis of prevalence and comparative studies.

J Appl Oral Sci. 2023

[2]
Molecular Mechanisms of Craniofacial and Dental Abnormalities in Osteopetrosis.

Int J Mol Sci. 2023-6-20

[3]
Prevalence of clinical signs, symptoms and comorbidities at diagnosis of acromegaly: a systematic review in accordance with PRISMA guidelines.

Pituitary. 2023-8

[4]
Paget's disease: a review of the epidemiology, etiology, genetics, and treatment.

Front Genet. 2023-4-26

[5]
Radiographic findings in acromegaly: pictorial essay.

Radiol Bras. 2023

[6]
Craniofacial Microsomia: New Updates in Spinal Anomalies.

J Craniofac Surg. 2023-6-1

[7]
Goldenhar Syndrome: An Atypical Presentation With Developmental and Speech Delay.

Cureus. 2023-3-16

[8]
Multiple Cemento-Ossifying Fibroma: A Sign of Hyperparathyroidism-Jaw Tumour Syndrome.

Case Rep Dent. 2023-3-8

[9]
Genetic association analysis of 77,539 genomes reveals rare disease etiologies.

Nat Med. 2023-3

[10]
Genomic Profiling of the Craniofacial Ossifying Fibroma by Next-Generation Sequencing.

Head Neck Pathol. 2023-9

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