Cargando…
SOFT Syndrome: The First Case in Iran
Primordial dwarfism (PD) is a group of rare genetically heterogeneous disorders consisted of disorders with intrauterine growth retardation continued through the life. SOFT syndrome with characteristics of short stature, onychodysplasia, facial dysmorphism, and hypotrichosis has been presented as a...
Autores principales: | Mostofizadeh, Neda, Gheidarloo, Mahshid, Hashemipour, Mahin, Dehkordi, Elham Hashemi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6159314/ https://www.ncbi.nlm.nih.gov/pubmed/30310776 http://dx.doi.org/10.4103/abr.abr_13_18 |
Ejemplares similares
-
Thrombotic Thrombocytopenic Purpura in a Child with Diabetic Ketoacidosis
por: Mostofizadeh, Neda, et al.
Publicado: (2018) -
Twin Brothers with Carnitine Membrane Transporter Deficiency: A Case Study
por: Dehkordi, Elham Hashemi, et al.
Publicado: (2018) -
Cardiovascular Risk Factors in Children and Adolescents with Congenital Adrenal Hyperplasia
por: Hashemi Dehkordi, Elham, et al.
Publicado: (2021) -
A Case of Tyrosinemia Type III with Status Epilepticus and Mental Retardation
por: Najafi, Reza, et al.
Publicado: (2018) -
The impact of poor glycemic control on lipid profile variables in children with type 1 diabetes mellitus
por: Mostofizadeh, Neda, et al.
Publicado: (2019)