One of the characteristics of kids with Dyggve syndrome is having

Case 14 at the age of 16 years. Note coarse facies and skeletal anomalies

Nager Syndrome — Nager Acrofacial Dysostosis: Symptoms & Causes

Frontiers Case Report: Precision genetic diagnosis in a case of Dyggve-Melchior-Clausen syndrome reveals paternal isodisomy and heterodisomy of chromosome 18 with imprinting clinical implications

Flowchart of the approach used in this study to investigate a group of

Tetrasomy 18p: case report and review of literature

Frontiers 16q24.3 Microduplication in a Patient With Developmental Delay, Intellectual Disability, Short Stature, and Nonspecific Dysmorphic Features: Case Report and Review of the Literature

PDF) Dyggve-Melchior-Clausen syndrome without mental retardation (Smith-McCort dysplasia)

Morquio Syndrome (Mucopolysaccharidosis Type IV) Differential Diagnoses

Genes, Free Full-Text

PDF) Dyggve-Melchior-Clausen syndrome without mental retardation (Smith-McCort dysplasia)

Frontiers Physical, language, neurodevelopment and phenotype-genotype correlation of Chinese patients with Mowat-Wilson syndrome

PDF) Mutations in a novel gene Dymeclin (FLJ20071) are responsible for Dyggve-Melchior-Clausen syndrome

(PDF) A Novel Homozygous Frameshift Variant in DYM Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients

Frequency of the main orthopedic manifestations in the studied