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Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease

BACKGROUND: Microcephalic osteodysplastic primordial dwarfism type II (MOPDII) is the most common form of primordial dwarfism, caused by bialleic mutations in the pericentrin gene (PCNT). Aside from its classic features, there are multiple associated medical complications, including a well-documente...

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Autores principales: Duker, Angela L., Kinderman, Dagmar, Jordan, Christy, Niiler, Tim, Baker-Smith, Carissa M., Thompson, Louise, Parry, David A., Carroll, Ricki S., Bober, Michael B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8139163/
https://www.ncbi.nlm.nih.gov/pubmed/34016138
http://dx.doi.org/10.1186/s13023-021-01852-y
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author Duker, Angela L.
Kinderman, Dagmar
Jordan, Christy
Niiler, Tim
Baker-Smith, Carissa M.
Thompson, Louise
Parry, David A.
Carroll, Ricki S.
Bober, Michael B.
author_facet Duker, Angela L.
Kinderman, Dagmar
Jordan, Christy
Niiler, Tim
Baker-Smith, Carissa M.
Thompson, Louise
Parry, David A.
Carroll, Ricki S.
Bober, Michael B.
author_sort Duker, Angela L.
collection PubMed
description BACKGROUND: Microcephalic osteodysplastic primordial dwarfism type II (MOPDII) is the most common form of primordial dwarfism, caused by bialleic mutations in the pericentrin gene (PCNT). Aside from its classic features, there are multiple associated medical complications, including a well-documented risk of neurovascular disease. Over the past several years, it has become apparent that additional vascular issues, as well as systemic hypertension and kidney disease may also be related to MOPDII. However, the frequency and extent of the vasculopathy was unclear. To help address this question, a vascular substudy was initiated within our Primordial Dwarfism Registry. RESULTS: Medical records from 47 individuals, living and deceased, ranging in age from 3 to 41years of age were interrogated for this purpose. Of the total group, 64% were diagnosed with moyamoya, intracranial aneurysms, or both. In general, the age at diagnosis for moyamoya was younger than aneurysms, but the risk for neurovascular disease was throughout the shortened lifespan. In addition to neurovascular disease, renal, coronary and external carotid artery involvement are documented. 43% of the total group was diagnosed with hypertension, and 17% had myocardial infarctions. A total of 32% of the entire cohort had some form of chronic kidney disease, with 4% of the total group necessitating a kidney transplant. In addition, 38% had diabetes/insulin resistance. Ages of diagnoses, treatment modalities employed, and location of vasculopathies were notated as available and applicable, as well as frequencies of other comorbidities. CONCLUSIONS: It is now clear that vascular disease in MOPDII is global and screening of the cardiac and renal vessels is warranted along with close monitoring of blood pressure. We recommend a blood pressure of 110/70mmHg as a starting point for an upper limit, especially if the individual has a history of neurovascular disease, chronic kidney disease and/or diabetes. Additionally, providers need to be at high alert for the possibility of myocardial infarctions in young adults with MOPDII, so that appropriate treatment can be initiated promptly in an acute situation.
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spelling pubmed-81391632021-05-25 Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease Duker, Angela L. Kinderman, Dagmar Jordan, Christy Niiler, Tim Baker-Smith, Carissa M. Thompson, Louise Parry, David A. Carroll, Ricki S. Bober, Michael B. Orphanet J Rare Dis Research BACKGROUND: Microcephalic osteodysplastic primordial dwarfism type II (MOPDII) is the most common form of primordial dwarfism, caused by bialleic mutations in the pericentrin gene (PCNT). Aside from its classic features, there are multiple associated medical complications, including a well-documented risk of neurovascular disease. Over the past several years, it has become apparent that additional vascular issues, as well as systemic hypertension and kidney disease may also be related to MOPDII. However, the frequency and extent of the vasculopathy was unclear. To help address this question, a vascular substudy was initiated within our Primordial Dwarfism Registry. RESULTS: Medical records from 47 individuals, living and deceased, ranging in age from 3 to 41years of age were interrogated for this purpose. Of the total group, 64% were diagnosed with moyamoya, intracranial aneurysms, or both. In general, the age at diagnosis for moyamoya was younger than aneurysms, but the risk for neurovascular disease was throughout the shortened lifespan. In addition to neurovascular disease, renal, coronary and external carotid artery involvement are documented. 43% of the total group was diagnosed with hypertension, and 17% had myocardial infarctions. A total of 32% of the entire cohort had some form of chronic kidney disease, with 4% of the total group necessitating a kidney transplant. In addition, 38% had diabetes/insulin resistance. Ages of diagnoses, treatment modalities employed, and location of vasculopathies were notated as available and applicable, as well as frequencies of other comorbidities. CONCLUSIONS: It is now clear that vascular disease in MOPDII is global and screening of the cardiac and renal vessels is warranted along with close monitoring of blood pressure. We recommend a blood pressure of 110/70mmHg as a starting point for an upper limit, especially if the individual has a history of neurovascular disease, chronic kidney disease and/or diabetes. Additionally, providers need to be at high alert for the possibility of myocardial infarctions in young adults with MOPDII, so that appropriate treatment can be initiated promptly in an acute situation. BioMed Central 2021-05-20 /pmc/articles/PMC8139163/ /pubmed/34016138 http://dx.doi.org/10.1186/s13023-021-01852-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Duker, Angela L.
Kinderman, Dagmar
Jordan, Christy
Niiler, Tim
Baker-Smith, Carissa M.
Thompson, Louise
Parry, David A.
Carroll, Ricki S.
Bober, Michael B.
Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease
title Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease
title_full Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease
title_fullStr Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease
title_full_unstemmed Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease
title_short Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease
title_sort microcephalic osteodysplastic primordial dwarfism type ii is associated with global vascular disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8139163/
https://www.ncbi.nlm.nih.gov/pubmed/34016138
http://dx.doi.org/10.1186/s13023-021-01852-y
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