The genetics of enuresis: A review

Journal of Urology

Volumn 166, Issue 6, 2001, Pages 2438-2443

  Von Gontard, Alexander ^a,b,c   Schaumburg, Henritte ^a,b,c   Hollmann, Elke ^a,b,c   Eiberg, Hans ^a,b,c   Rittig, Søren ^a,b,c  

^a UNIVERSITY OF COLOGNE   (Germany)

^b AARHUS UNIVERSITY HOSPITAL   (Denmark)

^c UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

Biochemical; Enuresis; Genetics; Linkage (genetics)

Indexed keywords

GENE PRODUCT;

ADOPTION; AUTOSOMAL DOMINANT INHERITANCE; CONFERENCE PAPER; DISEASE TRANSMISSION; ENVIRONMENTAL FACTOR; FAMILY STUDY; GENE LOCUS; GENE SEGREGATION; GENETIC LINKAGE; GENOTYPE; HEREDITY; HUMAN; MOLECULAR GENETICS; NOCTURNAL ENURESIS; PHARMACOGENETICS; PHENOTYPE; PRIORITY JOURNAL; TWINS; URGE INCONTINENCE;

EID: 0035174170     PISSN: 00225347     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-5347(05)65611-X     Document Type: Conference Paper

References (56)

1. Primary nocturnal enuresis in children. Background and treatment
2. Micturition habits and incontinence in 7-year-old Swedish school entrants
3. Urinary incontinence in children: Suggestions for definitions and terminology
4. Standardization and definitions in lower urinary tract dysfunction in children
5. Enuresis. A genetic study
6. Enuresis - A clinical and genetic study
7. Enuresis in children
8. The genetics of enuresis
9. Nocturnal enuresis: A familial condition
10. Treating bed wetting
11. Clinical enuresis phenotypes in familial nocturnal enuresis
12. Transmission of primary nocturnal enuresis and attention deficit hyperactivity disorder
13. Transmission of primary nocturnal enuresis and attention deficit hyperactivity disorder
14. Factors related to the age of attainment of nocturnal bladder control: An 8-year longitudinal study
15. Secondary enuresis in a birth cohort of New Zealand children
16. Enuresis in seven-year-old children
17. Nocturnal enuresis in twins
18. Enuresis in twins
19. Behavioural genetics of early childhood: Fears, restlessness, motion sickness and enuresis
20. Nocturnal enuresis in a nationwide twin cohort
21. Enuresis among kibbutz children
22. Zur Frage der Vererbung der Enuresis nocturna
23. Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q
24. Erblichkeit und Enuresis nocturna
25. The genetics of primary nocturnal enuresis: Inheritance and suggestion of a second major gene on chromosome 12q
26. Enuresis: Associations of genotype and phenotype
27. The genetics of nocturnal enuresis: A simple question of complexity
28. The role of family history in predicting response to desmopressin in nocturnal enuresis
29. Nocturnal enuresis: Experience with long-term use of intranasally administered desmopressin
30. Micturition habits and bladder capacity in normal children and in patients with desmopressin-resistant enuresis
31. No relationship between family history of enuresis and response to desmopressin
32. Response to desmopressin as a function of urine osmolality in the treatment of monosymptomatic nocturnal enuresis: A double-blind prospective study
33. Predictors of response to desmopressin in children and adolescents with monosymptomatic nocturnal enuresis
34. Exclusion mapping
35. Assignment of dominant inherited nocturnal enuresis to chromosome 13q. Evidence of genetic heterogeneity
36. Nocturnal enuresis is linked to a specific gene
37. Total genome scan analysis in a single extended family for primary nocturnal enuresis: Evidence for a new locus (ENUR3) for primary nocturnal enuresis on chromosome 22q11
38. Molecular genetics of nocturnal enuresis: Clinical and genetic heterogeneity
39. Molecular genetics of nocturnal enuresis: Linkage to a locus on chromosome 22
40. Dominant inheritance for a gene which mainly causes urge incontinence in a large four generation Danish family
41. Genetic association studies in behavioural neuroscience
42. Assignment of GUCY1B2, the gene coding for the beta2 subunit of human guanylyl cyclase to chromosomal band 13q14.3 between markers D13S168 and D13S155
43. The Acquaporin-2 water channel gene is not mutated in families with primary nocturnal enuresis, in which the disease cosegregates with chromosome 12q
44. Human TRH-degrading ectoenzyme cDNA cloning, functional expression, genomic structure and chromosomal assignment
45. Das Gen-Konzept, Phaenogenetik
46. Why behavioural phenotypes?
47. The genetic contribution to the phenotype
48. Nocturnal enuresis at the molecular level
49. Prepulse inhibition of startle and the neurobiology of primary nocturnal enuresis
50. Is dysco-ordinated voiding in children an hereditary disorder?
51. Primary nocturnal enuresis: A urodynamic study spanning three generations
52. Successful treatment of giggle incontinence with methylphenidate
53. Treatment of enuresis risoria in children by self-administered electric and imaginary shock