Literature DB >> 8071971

Segregation analysis of Alagille syndrome.

S Dhorne-Pollet1, J F Deleuze, M Hadchouel, C Bonaïti-Pellié.   

Abstract

Alagille syndrome (AGS) is a well defined genetic disorder characterised by five major features. An autosomal dominant mode of transmission with reduced penetrance has been suggested by the analysis of a limited number of families. However there has been no statistical analysis. We report here the first segregation analysis of AGS, using 33 families collected through 43 probands. Segregation analysis of these families allowed us to conclude that AGS is transmitted as a dominant disorder with 94% penetrance and 15% of cases are sporadic. The expressivity of the phenotype was variable and 26 persons (15 parents and 11 sibs) were identified as presenting minor forms of the disease. These results are valuable for genetic counselling.

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Mesh:

Year:  1994        PMID: 8071971      PMCID: PMC1049922          DOI: 10.1136/jmg.31.6.453

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  28 in total

1.  Genetic tests under incomplete ascertainment.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1959-03       Impact factor: 11.025

2.  [Multiple congenital malformations in a boy with a chromosome abnormality of the group F (46-XY, 20-P), the son of a clinically healthy subject with an analogous chromosome malformation].

Authors:  G Loiodice; D G Rovetta; G Bellicini; G Callura; F Bergamo
Journal:  Minerva Pediatr       Date:  1970-05-26       Impact factor: 1.312

3.  [Congenital stenosis of the pulmonary artery and its collaterals. Apropos of 20 cases].

Authors:  J C Hoeffel; M Henry; J Jimenez; C Pernot
Journal:  Arch Fr Pediatr       Date:  1973-11

4.  Intrahepatic "cholestasis facies": is it specific for Alagille syndrome?

Authors:  R J Sokol; J E Heubi; W F Balistreri
Journal:  J Pediatr       Date:  1983-08       Impact factor: 4.406

5.  Arteriohepatic dysplasia: a benign syndrome of intrahepatic cholestasis with multiple organ involvement.

Authors:  C A Riely; E Cotlier; P S Jensen; G Klatskin
Journal:  Ann Intern Med       Date:  1979-10       Impact factor: 25.391

6.  Arteriohepatic dysplasia (Alagille syndrome): extreme variability among affected family members.

Authors:  S A Shulman; J S Hyams; R Gunta; R M Greenstein; S B Cassidy
Journal:  Am J Med Genet       Date:  1984-10

7.  Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur.

Authors:  D Alagille; M Odièvre; M Gautier; J P Dommergues
Journal:  J Pediatr       Date:  1975-01       Impact factor: 4.406

8.  Four generations of arteriohepatic dysplasia.

Authors:  D R LaBrecque; F A Mitros; R J Nathan; K G Romanchuk; G F Judisch; G H El-Khoury
Journal:  Hepatology       Date:  1982 Jul-Aug       Impact factor: 17.425

9.  Renal lipidosis associated with arteriohepatic dysplasia (Alagille's syndrome).

Authors:  M Chung-Park; M Petrelli; A S Tavill; P W Hall; M S Henoch; B B Dahms
Journal:  Clin Nephrol       Date:  1982-12       Impact factor: 0.975

10.  Studies of the aetiology of neonatal hepatitis and biliary atresia.

Authors:  D M Danks; P E Campbell; I Jack; J Rogers; A L Smith
Journal:  Arch Dis Child       Date:  1977-05       Impact factor: 3.791

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  14 in total

Review 1.  Alagille syndrome: pathogenesis, diagnosis and management.

Authors:  Peter D Turnpenny; Sian Ellard
Journal:  Eur J Hum Genet       Date:  2011-09-21       Impact factor: 4.246

2.  Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families.

Authors:  I D Krantz; R P Colliton; A Genin; E B Rand; L Li; D A Piccoli; N B Spinner
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

3.  Alagille syndrome: family studies.

Authors:  F V Elmslie; A J Vivian; H Gardiner; C Hall; A P Mowat; R M Winter
Journal:  J Med Genet       Date:  1995-04       Impact factor: 6.318

Review 4.  Alagille syndrome.

Authors:  I D Krantz; D A Piccoli; N B Spinner
Journal:  J Med Genet       Date:  1997-02       Impact factor: 6.318

5.  Paucity of intrahepatic bile ducts, solitary kidney and atrophic pancreas with diabetes mellitus: atypical Alagille syndrome?

Authors:  K Devriendt; L Dooms; W Proesmans; F de Zegher; V Desmet; E Eggermont
Journal:  Eur J Pediatr       Date:  1996-02       Impact factor: 3.183

6.  Molecular analysis of 24 Alagille syndrome families identifies a single submicroscopic deletion and further localizes the Alagille region within 20p12.

Authors:  E B Rand; N B Spinner; D A Piccoli; P F Whitington; R Taub
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

7.  [Endocrinologic and metabolic complications of Alagille syndrome].

Authors:  L C Hofbauer; A Mrozek-Lasota; T Jelinek; H D Schworm; D Zimmermann; A E Heufelder
Journal:  Med Klin (Munich)       Date:  1997-09-15

8.  Deleted chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genes.

Authors:  J F Deleuze; S Dhorne; J Hazan; E Borghi; N Raynaud; N Pollet; M Meunier-Rotival; J Deschatrette; D Alagille; M Hadchouel
Journal:  Mamm Genome       Date:  1994-11       Impact factor: 2.957

9.  Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family.

Authors:  F A Hol; B C Hamel; M P Geurds; I Hansmann; F A Nabben; O Daniëls; E C Mariman
Journal:  Hum Genet       Date:  1995-06       Impact factor: 4.132

10.  Alagille syndrome: Genetics and Functional Models.

Authors:  Melissa A Gilbert; Nancy B Spinner
Journal:  Curr Pathobiol Rep       Date:  2017-09
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