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Craniofacial and Craniocervical Features in Cartilage-Hair Hypoplasia: A Radiological Study of 17 Patients and 34 Controls

BACKGROUND: Biallelic mutations in the non-coding RNA gene RMRP cause Cartilage-hair hypoplasia (CHH), a rare skeletal dysplasia in which the main phenotypic characteristic is severe progressive growth retardation. OBJECTIVE: This study compared the cranial dimensions of individuals with CHH to heal...

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Autores principales: Arponen, Heidi, Evälahti, Marjut, Mäkitie, Outi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8703216/
https://www.ncbi.nlm.nih.gov/pubmed/34956076
http://dx.doi.org/10.3389/fendo.2021.741548
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author Arponen, Heidi
Evälahti, Marjut
Mäkitie, Outi
author_facet Arponen, Heidi
Evälahti, Marjut
Mäkitie, Outi
author_sort Arponen, Heidi
collection PubMed
description BACKGROUND: Biallelic mutations in the non-coding RNA gene RMRP cause Cartilage-hair hypoplasia (CHH), a rare skeletal dysplasia in which the main phenotypic characteristic is severe progressive growth retardation. OBJECTIVE: This study compared the cranial dimensions of individuals with CHH to healthy subjects. METHODS: Lateral skull radiographs of 17 patients with CHH (age range 10 to 59 years) and 34 healthy individuals (age range 10 to 54 years) were analyzed for relative position of the jaws to skull base, craniofacial height and depth, as well as vertical growth pattern of the lower jaw, anterior cranial base angle, and the relationship between the cervical spine and skull base. RESULTS: We found that the length of the upper and lower jaws, and clivus were significantly decreased in patients with CHH as compared to the controls. Anterior cranial base angle was large in patients with CHH. Basilar invagination was not found. CONCLUSION: This study found no severe craniofacial involvement of patients with CHH, except for the short jaws. Unexpectedly, mandibular deficiency did not lead to skeletal class II malocclusion. CLINICAL IMPACT: Although the jaws were shorter in patients with CHH, they were proportional to each other. A short posterior cranial base was not associated with craniocervical junction pathology.
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spelling pubmed-87032162021-12-25 Craniofacial and Craniocervical Features in Cartilage-Hair Hypoplasia: A Radiological Study of 17 Patients and 34 Controls Arponen, Heidi Evälahti, Marjut Mäkitie, Outi Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Biallelic mutations in the non-coding RNA gene RMRP cause Cartilage-hair hypoplasia (CHH), a rare skeletal dysplasia in which the main phenotypic characteristic is severe progressive growth retardation. OBJECTIVE: This study compared the cranial dimensions of individuals with CHH to healthy subjects. METHODS: Lateral skull radiographs of 17 patients with CHH (age range 10 to 59 years) and 34 healthy individuals (age range 10 to 54 years) were analyzed for relative position of the jaws to skull base, craniofacial height and depth, as well as vertical growth pattern of the lower jaw, anterior cranial base angle, and the relationship between the cervical spine and skull base. RESULTS: We found that the length of the upper and lower jaws, and clivus were significantly decreased in patients with CHH as compared to the controls. Anterior cranial base angle was large in patients with CHH. Basilar invagination was not found. CONCLUSION: This study found no severe craniofacial involvement of patients with CHH, except for the short jaws. Unexpectedly, mandibular deficiency did not lead to skeletal class II malocclusion. CLINICAL IMPACT: Although the jaws were shorter in patients with CHH, they were proportional to each other. A short posterior cranial base was not associated with craniocervical junction pathology. Frontiers Media S.A. 2021-12-10 /pmc/articles/PMC8703216/ /pubmed/34956076 http://dx.doi.org/10.3389/fendo.2021.741548 Text en Copyright © 2021 Arponen, Evälahti and Mäkitie https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Arponen, Heidi
Evälahti, Marjut
Mäkitie, Outi
Craniofacial and Craniocervical Features in Cartilage-Hair Hypoplasia: A Radiological Study of 17 Patients and 34 Controls
title Craniofacial and Craniocervical Features in Cartilage-Hair Hypoplasia: A Radiological Study of 17 Patients and 34 Controls
title_full Craniofacial and Craniocervical Features in Cartilage-Hair Hypoplasia: A Radiological Study of 17 Patients and 34 Controls
title_fullStr Craniofacial and Craniocervical Features in Cartilage-Hair Hypoplasia: A Radiological Study of 17 Patients and 34 Controls
title_full_unstemmed Craniofacial and Craniocervical Features in Cartilage-Hair Hypoplasia: A Radiological Study of 17 Patients and 34 Controls
title_short Craniofacial and Craniocervical Features in Cartilage-Hair Hypoplasia: A Radiological Study of 17 Patients and 34 Controls
title_sort craniofacial and craniocervical features in cartilage-hair hypoplasia: a radiological study of 17 patients and 34 controls
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8703216/
https://www.ncbi.nlm.nih.gov/pubmed/34956076
http://dx.doi.org/10.3389/fendo.2021.741548
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