Multiple pterygium syndrome with marked pterygia of the fingers and MRI changes in the spine - ScienceDirect
Manejo quirúrgico de la deformidad vertebral en un paciente con síndrome de Escobar: revisión de la literatura
Genes | Free Full-Text | The Clinical and Genotypic Spectrum of Scoliosis in Multiple Pterygium Syndrome: A Case Series on 12 Children
Multiple pterygium syndrome: MedlinePlus Genetics
Owen Sedey
Escobar Syndrome—An Multidisciplinary Approach for an Excellent Outcome With 3 Years of Follow-Up | Semantic Scholar
Escobar Syndrome Affecting Two Male Siblings in a Family: A Rare Case Report | Semantic Scholar
Amazing Grace
Mutations in the Embryonal Subunit of the Acetylcholine Receptor (CHRNG) Cause Lethal and Escobar Variants of Multiple Pterygium Syndrome - ScienceDirect
Escobar Syndrome Associated with Spine and Orthopedic Pathologies: Case Reports and Literature Review
Escobar Syndrome | Neuromuscular Disorders West Palm Beach, FL | Spine Specialist New York, NY
Radiological imaging and photos of patients with Escobar syndrome: (A)... | Download Scientific Diagram
The first case, a 17-year-old male patient whose brother also had... | Download Scientific Diagram
I am having a 24hr Ph... - Roxy Anderson - Escobar Syndrome | Facebook
PDF) Escobar Syndrome Associated with Spine and Orthopedic Pathologies: Case Reports and Literature Review
New publication: CHRNG-related nonlethal multiple pterygium syndrome: Muscle imaging pattern and clinical, histopathological, and molecular genetic findings - latest neuromuscular research updates - Lochmüller Lab
This is one thing... - Roxy Anderson - Escobar Syndrome | Facebook
Chronic Abdominal Pain in a Patient with Escobar Syndrome | Semantic Scholar
Multiple Pterygium Syndrome | SpringerLink
Escobar syndrome in three male patients of same family – ScienceOpen
Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3. - Abstract - Europe PMC
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Homozygous intronic variants in TPM2 cause recessively inherited Escobar variant of multiple pterygium syndrome and congenital myopathy - ScienceDirect