has material basis in germline mutation in SCARF2 van den Ende-Gupta syndrome https://www.malacards.org/card/van_den_ende_gupta_syndrome OMIM:600920 Orphanet:2460 SCTID:719845008 GARD:0003382 Marden Walker like syndrome Van den Ende Gupta syndrome Marden-Walker-like syndrome without psychomotor retardation MESH:C535909 van den Ende-Gupta syndrome Marden-Walker-like syndrome DOID:0111699 VAN DEN Ende-Gupta syndrome VDEGS icd11.foundation:1740735985 MEDGEN:322127 Van den Ende-Gupta syndrome is a very rare syndrome characterized by blepharophimosis, arachnodactyly, joint contractures, and characteristic dysmorphic features. blepharophimosis, arachnodactyly, and congenital contractures Marden Walker like syndrome without psychomotor retardation UMLS:C1833136 MONDO:0010959 multiple congenital anomalies/dysmorphic syndrome without intellectual disability arthrogryposis multiplex congenita obsolete syndrome or malformation associated with head and neck malformations