Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypes. Issue 5 (21st April 2018)

• Record Type: Journal Article
• Authors: Ivanovski, Ivan; Akbaroghli, Susan; Pollazzon, Marzia; Gelmini, Chiara; Caraffi, Stefano Giuseppe; Mansouri, Mahboubeh; Chavoshzadeh, Zahra; Rosato, Simonetta; Polizzi, Valeria; Gargano, Giancarlo; Alders, Marielle; Garavelli, Livia; Hennekam, Raoul C.
• Is Part Of: American journal of medical genetics. Volume 176:Issue 5(2018)
• Page Start: 1166
• Page End: 1174
• Publication Date: 2018-04-21
• Subjects: ADAMTS3 -- CCBE1 -- DCHS1 -- FAT4 -- Hennekam syndrome -- lymphedema -- Van Maldergem syndrome; Medical genetics -- Periodicals; 616.14205
• DOI: 10.1002/ajmg.a.38652
• Languages: English
• ISSNs: 1552-4825

Abstract

Abstract : Biallelic variants in FAT4 are associated with the two disorders, Van Maldergem syndrome (VMS) ( n = 11) and Hennekam syndrome (HS) ( n = 40). Both conditions are characterized by a typical facial gestalt and mild to moderate intellectual disability, but differ in the occurrence of neonatal hypotonia and feeding problems, hearing loss, tracheal anomalies, and osteopenia in VMS, and lymphedema in HS. VMS can be caused by autosomal recessive variants in DCHS1 as well, and HS can also be caused by autosomal recessive variants in CCBE1 and ADAMTS3 . Here we report two siblings with VMS and one girl with HS, all with FAT4 variants, and provide an overview of the clinical findings in all patients reported with FAT4 variants. Our comparison of the complete phenotypes of patients with VMS and HS indicates a resemblance of several signs, but differences in several other main signs and symptoms, each of marked importance for affected individuals.