Clinical Findings and Dental Manifestations Associated With Microcephalic Osteodysplastic Primordial Dwarfism Type II: A Case Report
Background: Microcephalic Osteodysplastic Primordial Dwarfism type 2 (MOPD II) is a rare untreatable genetic disorder characterized by severe prenatal and postnatal growth retardation, microcephaly, bird-headed face (receding forehead and chin, a beaklike nose, and prominent eyes), skeletal abnormal...
Main Authors: | Bahareh Nazemi Salman, Nazila Biglar, Masoumeh Mirkeshavarz, Ghasem Ansari |
---|---|
Format: | Article |
Language: | English |
Published: |
Mazandaran University of Medical Sciences
2022-12-01
|
Series: | Journal of Pediatrics Review |
Subjects: | |
Online Access: | http://jpr.mazums.ac.ir/article-1-479-en.html |
Similar Items
-
Case Report: short stature, kidney anomalies, and cerebral aneurysms in a novel homozygous mutation in the PCNT gene associated with microcephalic osteodysplastic primordial dwarfism type II
by: Maddalena Petraroli, et al.
Published: (2023-05-01) -
MAJEWSKI OSTEODYSPLASTIC PRIMORDIAL DWARFISM TYPE II: CLINICAL FINDINGS AND DENTAL MANAGEMENT OF A CHILD PATIENT
by: Arslan Terlemez, et al.
Published: (2015-01-01) -
Microcephalic osteodysplastic primordial dwarfism type II and Klinefelter syndrome: report of two competing growth syndromes
by: AlAnoud Al-Jarbou, et al.
Published: (2018-06-01) -
In‐frame deletion of SMC5 related with the phenotype of primordial dwarfism, chromosomal instability and insulin resistance
by: Wenjiao Zhu, et al.
Published: (2023-01-01) -
ORO-DENTAL MANIFESTATIONS IN A CHILD WITH VISCERAL DWARFISM
by: Gabriela Păduraru, et al.
Published: (2016-01-01)