Van den Ende-Gupta syndrome

Summary
Synonym
  • Marden-Walker-like syndrome
  • Marden-Walker-like syndrome without psychmotor retardation
  • VDEGS
  • blepharophimosis, arachnodactyly, and congenital contractures
Definition
A syndrome characterized by severe contractual arachnodactyly, distinctive facial features, blepharophimosis, and absence of neurological involvement that has_material_basis_in homozygous or compound heterozygous mutation in the SCARF2 gene on chromosome 22q11.21.
Super Class
autosomal recessive disease syndrome
Disease Ontology
DOID:0111699
Mondo Disease Ontology
MeSH
UMLS
ORDO
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
91179 SCARF2 scavenger receptor class F member 2
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q96GP6 Scavenger receptor class F member 2

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026