An Iranian Patient with Maroteaux Type Acromesomelic Dysplasia, Showing no Involvement of Distal Lower Limbs

J Clin Res Pediatr Endocrinol. 2020 Mar 19;12(1):122-123. doi: 10.4274/jcrpe.galenos.2019.2019.0090. Epub 2019 Jul 24.

Authors

Hossein Moravej^{1

2}, Mozhagn Moghtaderi¹, Sara Mostafavi³

Affiliations

¹ Shiraz University of Medical Sciences, Neonatal Research Center, Department of Pediatrics, Shiraz, Iran
² Shiraz University of Medical Sciences, Department of Pediatric Endocrinology, Shiraz, Iran
³ Shiraz University of Medical Sciences, Student Research Committee, Shiraz, Iran

PMID: 31339259
PMCID: PMC7127880
DOI: 10.4274/jcrpe.galenos.2019.2019.0090

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Bone Diseases, Developmental / diagnosis*
Bone Diseases, Developmental / genetics
Bone Diseases, Developmental / pathology
Child, Preschool
Humans
Iran
Male

Supplementary concepts

Acromesomelic dysplasia, Maroteaux type