KEGG   DISEASE: FDLAB syndrome
Entry
H02255                      Disease                                
Name
FDLAB syndrome;
Traboulsi syndrome
Description
Facial dysmorphism, lens dislocation, anterior-segment abnormalities, and spontaneous filtering blebs (FDLAB) syndrome, also known as Traboulsi syndrome, is an autosomal recessive disorder. FDLAB syndrome is caused by mutations in ASPH that encodes aspartyl/asparaginyl beta-hydroxylase.
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
    H02255  FDLAB syndrome
Gene
ASPH [HSA:444] [KO:K00476]
Other DBs
ICD-11: LD2F.1Y
ICD-10: Q87.0
OMIM: 601552
Reference
  Authors
Patel N, Khan AO, Mansour A, Mohamed JY, Al-Assiri A, Haddad R, Jia X, Xiong Y, Megarbane A, Traboulsi EI, Alkuraya FS
  Title
Mutations in ASPH cause facial dysmorphism, lens dislocation, anterior-segment abnormalities, and spontaneous filtering blebs, or Traboulsi syndrome.
  Journal
Am J Hum Genet 94:755-9 (2014)
DOI:10.1016/j.ajhg.2014.04.002
Reference
  Authors
Mansour AM, Younis MH, Dakroub RH
  Title
Anterior segment imaging and treatment of a case with syndrome of ectopia lentis, spontaneous filtering blebs, and craniofacial dysmorphism.
  Journal
Case Rep Ophthalmol 4:84-90 (2013)
DOI:10.1159/000350951
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