▷ Is Autosomal recessive multiple pterygium syndrome / Escobar syndrome hereditary?
تويتر \ American Cleft Palate Craniofacial Association على تويتر: "Escobar Syndrome—An Multidisciplinary Approach for an Excellent Outcome With 3 Years of Follow-Up #EscobarSyndrome https://t.co/dVnCGs45gK https://t.co/NVtsfPJoQd"
Multiple pterygium syndrome: MedlinePlus Genetics
Indian Pediatrics - Editorial
Homozygous intronic variants in TPM2 cause recessively inherited Escobar variant of multiple pterygium syndrome and congenital myopathy - Neuromuscular Disorders
Escobar syndrome with monodactyly: A rare case report
Brave 14-year-old with a rare joint condition has had to endure 33 SURGERIES | Daily Mail Online
Escobar Syndrome Affecting Two Male Siblings in a Family: A Rare Case Report | Semantic Scholar
Escobar Syndrome Affecting Two Male Siblings in a Family: A Rare Case Report | Semantic Scholar
Neuromotor synapses in Escobar syndrome - Robinson - 2013 - American Journal of Medical Genetics Part A - Wiley Online Library
Case 1: 3-year old male with multiple pterygium syndrome of Escobar. | Download Scientific Diagram
Multiple pterygium syndrome with marked pterygia of the fingers and MRI changes in the spine - ScienceDirect
Grace
Escobar Syndrome Affecting Two Male Siblings in a Family: A Rare Case Report | Semantic Scholar
Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit - ScienceDirect
Radiological imaging and photos of patients with Escobar syndrome: (A)... | Download Scientific Diagram
Amazing Grace
Airway management in Escobar syndrome: A formidable challeng
Anesthesic Management for Escobar Syndrome: Case Report
Escobar Syndrome Associated with Spine and Orthopedic Pathologies: Case Reports and Literature Review
Neuromotor synapses in Escobar syndrome - Robinson - 2013 - American Journal of Medical Genetics Part A - Wiley Online Library
Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3. - Abstract - Europe PMC
ESCOBAR SYNDROME - Famagusta News
Truncating CHRNG mutations associated with interfamilial variability of the severity of the Escobar variant of multiple pterygium syndrome | BMC Genomic Data | Full Text
Owen Sedey
