KEGG   DISEASE: Yuksel-Vogel-Bauer syndrome
Entry
H02710                      Disease                                
Name
Yuksel-Vogel-Bauer syndrome
Description
Yuksel-Vogel-Bauer syndrome (YUVOB) is a multisystemic disorder caused by mutations in DLG5. Patients have a variety of phenotypes including cystic kidneys, nephrotic syndrome, hydrocephalus, limb abnormalities, congenital heart disease and craniofacial malformations. DLG5 is a member of the membrane-associated guanylate kinase family of proteins and participates in regulation of Hippo, sonic Hedgehog, and TGF beta signaling.
Category
Congenital malformation
Brite
Human diseases in ICD-11 classification [BR:br08403]
 20 Developmental anomalies
  Multiple developmental anomalies or syndromes
   LD2F  Syndromes with multiple structural anomalies, without predominant body system involvement
    H02710  Yuksel-Vogel-Bauer syndrome
Gene
DLG5 [HSA:9231] [KO:K24050]
Other DBs
ICD-11: LD2F.Y
ICD-10: Q87.8
OMIM: 620703
Reference
  Authors
Marquez J, Mann N, Arana K, Deniz E, Ji W, Konstantino M, Mis EK, Deshpande C, Jeffries L, McGlynn J, Hugo H, Widmeier E, Konrad M, Tasic V, Morotti R, Baptista J, Ellard S, Lakhani SA, Hildebrandt F, Khokha MK
  Title
DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes.
  Journal
J Med Genet 58:453-464 (2021)
DOI:10.1136/jmedgenet-2019-106805
Reference
  Authors
Yuksel Z, Vogel F, Alhashem AM, Alanzi TSA, Tabarki B, Kampe K, Kandaswamy KK, Werber M, Bertoli-Avella AM, Beetz C, Rolfs A, Bauer P
  Title
A homozygous frameshift variant in an alternatively spliced exon of DLG5 causes hydrocephalus and renal dysplasia.
  Journal
Clin Genet 95:631-633 (2019)
DOI:10.1111/cge.13513
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