E-ISSN 1658-8088 | ISSN 1658-807X
 

Case Report 


Opsismodysplasia and Dilated Cardiomyopathy: a case report

Muneer Almutairi, Mohammed Almannai.


Abstract
Background: Opsismodysplasia (OPSMD) is an extremely rare and severe autosomal recessive skeletal dysplasia that is under the category of severe spondylodysplastic dysplasia. It is characterized by delayed bone maturation, and affected patients are identified by a peculiar craniofacioskeletal dysmorphism in the form of wide anterior fontanelle, depressed nasal bridge, anteverted nares, and short limbs and feet. Radiologically, they are characterized by severe platyspondyly, squared metacarpals, delayed skeletal ossification, and metaphyseal cupping.
Case Presentation: We present the clinical and radiological features of a 14-month-old boy with a homozygous, likely pathogenic variant in INPPL1 gene c.2627dup (p.Pro977Thrfs*7) consistent with the diagnosis of OPSMD. He also has dilated cardiomyopathy.
Conclusion: OPSMD is an uncommon form of skeletal dysplasia that should be suspected in the context of short stature with characteristic radiological features. Up to now, no definitive therapeutic measures are available, and hence preventive measures are essential in the management of families with affected members.

Key words: Opsismodysplasia, hypophosphatemic chondrodysplasia, osteodystrophy, cardiomyopathy, case report.


 
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Pubmed Style

Almutairi M, Almannai M. Opsismodysplasia and Dilated Cardiomyopathy: a case report. JBCGenetics. 2020; 3(2): 100-103. doi:10.24911/JBCGenetics/183-1595951481


Web Style

Almutairi M, Almannai M. Opsismodysplasia and Dilated Cardiomyopathy: a case report. https://www.jbcgenetics.com/?mno=114413 [Access: March 14, 2024]. doi:10.24911/JBCGenetics/183-1595951481


AMA (American Medical Association) Style

Almutairi M, Almannai M. Opsismodysplasia and Dilated Cardiomyopathy: a case report. JBCGenetics. 2020; 3(2): 100-103. doi:10.24911/JBCGenetics/183-1595951481



Vancouver/ICMJE Style

Almutairi M, Almannai M. Opsismodysplasia and Dilated Cardiomyopathy: a case report. JBCGenetics. (2020), [cited March 14, 2024]; 3(2): 100-103. doi:10.24911/JBCGenetics/183-1595951481



Harvard Style

Almutairi, M. & Almannai, . M. (2020) Opsismodysplasia and Dilated Cardiomyopathy: a case report. JBCGenetics, 3 (2), 100-103. doi:10.24911/JBCGenetics/183-1595951481



Turabian Style

Almutairi, Muneer, and Mohammed Almannai. 2020. Opsismodysplasia and Dilated Cardiomyopathy: a case report. Journal of Biochemical and Clinical Genetics, 3 (2), 100-103. doi:10.24911/JBCGenetics/183-1595951481



Chicago Style

Almutairi, Muneer, and Mohammed Almannai. "Opsismodysplasia and Dilated Cardiomyopathy: a case report." Journal of Biochemical and Clinical Genetics 3 (2020), 100-103. doi:10.24911/JBCGenetics/183-1595951481



MLA (The Modern Language Association) Style

Almutairi, Muneer, and Mohammed Almannai. "Opsismodysplasia and Dilated Cardiomyopathy: a case report." Journal of Biochemical and Clinical Genetics 3.2 (2020), 100-103. Print. doi:10.24911/JBCGenetics/183-1595951481



APA (American Psychological Association) Style

Almutairi, M. & Almannai, . M. (2020) Opsismodysplasia and Dilated Cardiomyopathy: a case report. Journal of Biochemical and Clinical Genetics, 3 (2), 100-103. doi:10.24911/JBCGenetics/183-1595951481





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