KEGG   DISEASE: Congenital hydrocephalus
Entry
H01677                      Disease                                
Name
Congenital hydrocephalus
  Subgroup
X-linked hydrocephalus [DS:H02458]
Congenital communicating hydrocephalus (HYDCC)
Normal-pressure hydrocephalus (HYDNP)
Description
Congenital hydrocephalus (HYC) is a common birth defect in the circulation of the cerebrospinal fluid (CSF). It is characterized by ventricular dilatation. Although commonly considered a single disorder, hydrocephalus is a collection of a heterogeneous complex and multifactorial disorders. It may occur alone (non-syndromic) or as part of a syndrome with other anomalies. Almost 50% of all cases of hydrocephalus are congenital and these are usually associated with adverse neurological outcome. It is probably the consequence of abnormal brain development. Genetic factors are involved in the pathogenesis of this disease. Molecular genetic studies have revealed that the responsible gene for X-linked human congenital hydrocephalus is encoding for L1CAM. Although the recurrence risk for congenital hydrocephalus excluding X-linked hydrocephalus is low, recently, a few genes for autosomal recessive congenital hydrocephalus have been identified. Besides genetic factors, many other factors influence the development of congenital hydrocephalus, such as congenital malformations, intracerebral hemorrhage, maternal alcohol use, infection, and X-ray radiation during pregnancy.
Category
Congenital malformation
Brite
Human diseases in ICD-11 classification [BR:br08403]
 20 Developmental anomalies
  Structural developmental anomalies primarily affecting one body system
   Structural developmental anomalies of the nervous system
    LA04  Congenital hydrocephalus
     H01677  Congenital hydrocephalus
Pathway
hsa04530  Tight junction
Gene
(HYC1) CCDC88C [HSA:440193] [KO:K25811]
(HYC2) MPDZ [HSA:8777] [KO:K06095]
(HYC3) WDR81 [HSA:124997] [KO:K17601]
(HYC4/HYDCC1) TRIM71 [HSA:131405] [KO:K12035]
(HYC5) SMARCC1 [HSA:6599] [KO:K11649]
(HYDNP1) CFAP43 [HSA:80217] [KO:K24223]
Other DBs
ICD-11: LA04
ICD-10: Q03
MeSH: D006849
OMIM: 236600 615219 617967 307000 618667 620241 236690
Reference
  Authors
Zhang J, Williams MA, Rigamonti D
  Title
Genetics of human hydrocephalus.
  Journal
J Neurol 253:1255-66 (2006)
DOI:10.1007/s00415-006-0245-5
Reference
PMID:23042809 (HYC1)
  Authors
Drielsma A, Jalas C, Simonis N, Desir J, Simanovsky N, Pirson I, Elpeleg O, Abramowicz M, Edvardson S
  Title
Two novel CCDC88C mutations confirm the role of DAPLE in autosomal recessive congenital hydrocephalus.
  Journal
J Med Genet 49:708-12 (2012)
DOI:10.1136/jmedgenet-2012-101190
Reference
PMID:23240096 (HYC2)
  Authors
Al-Dosari MS, Al-Owain M, Tulbah M, Kurdi W, Adly N, Al-Hemidan A, Masoodi TA, Albash B, Alkuraya FS
  Title
Mutation in MPDZ causes severe congenital hydrocephalus.
  Journal
J Med Genet 50:54-8 (2013)
DOI:10.1136/jmedgenet-2012-101294
Reference
PMID:33724704 (HYC3)
  Authors
Su J, Lu W, Li M, Zhang Q, Chen F, Yi S, Yang Q, Yi S, Zhou X, Huang L, Shen Y, Luo J, Qin Z
  Title
Novel compound heterozygous frameshift variants in WDR81 associated with congenital hydrocephalus 3 with brain anomalies: First Chinese prenatal case confirms WDR81 involvement.
  Journal
Mol Genet Genomic Med 9:e1624 (2021)
DOI:10.1002/mgg3.1624
Reference
PMID:29983323 (HYC4_5)
  Authors
Furey CG, Choi J, Jin SC, Zeng X, Timberlake AT, Nelson-Williams C, Mansuri MS, Lu Q, Duran D, Panchagnula S, Allocco A, Karimy JK, Khanna A, Gaillard JR, DeSpenza T, Antwi P, Loring E, Butler WE, Smith ER, Warf BC, Strahle JM, Limbrick DD, Storm PB, Heuer G, Jackson EM, Iskandar BJ, Johnston JM, Tikhonova I, Castaldi C, Lopez-Giraldez F, Bjornson RD, Knight JR, Bilguvar K, Mane S, Alper SL, Haider S, Guclu B, Bayri Y, Sahin Y, Apuzzo MLJ, Duncan CC, DiLuna ML, Gunel M, Lifton RP, Kahle KT
  Title
De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus.
  Journal
Neuron 99:302-314.e4 (2018)
DOI:10.1016/j.neuron.2018.06.019
Reference
PMID:31004071 (HYDNP1)
  Authors
Morimoto Y, Yoshida S, Kinoshita A, Satoh C, Mishima H, Yamaguchi N, Matsuda K, Sakaguchi M, Tanaka T, Komohara Y, Imamura A, Ozawa H, Nakashima M, Kurotaki N, Kishino T, Yoshiura KI, Ono S
  Title
Nonsense mutation in CFAP43 causes normal-pressure hydrocephalus with ciliary abnormalities.
  Journal
Neurology 92:e2364-e2374 (2019)
DOI:10.1212/WNL.0000000000007505
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