Literature DB >> 14684686

Consequences of JAG1 mutations.

B M Kamath1, L Bason, D A Piccoli, I D Krantz, N B Spinner.   

Abstract

BACKGROUND: Alagille syndrome (AGS) is a multi-system, autosomal dominant disorder with highly variable expressivity, caused by mutations within the Jagged1 (JAG1) gene.
METHODS: We studied 53 mutation positive relatives of 34 AGS probands to ascertain the frequency of clinical findings in JAG1 mutation carriers.
RESULTS: Eleven of 53 (21%) mutation positive relatives had clinical features that would have led to a diagnosis of AGS. Seventeen of the 53 (32%) relatives had mild features of AGS, revealed only after targeted evaluation following the diagnosis of a proband in their family. Twenty five of the 53 (47%) mutation positive relatives did not meet clinical criteria, and two of these individuals had no features consistent with AGS at all. The frequency of cardiac and liver disease was notably lower in the relatives than in the probands, characterising the milder end of the phenotypic spectrum. The characteristic facies of AGS was the feature with the highest penetrance, occurring almost universally in mutation positive probands and relatives.
CONCLUSIONS: This study has implications for genetic counselling of families with AGS and JAG1 mutations.

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Year:  2003        PMID: 14684686      PMCID: PMC1735339          DOI: 10.1136/jmg.40.12.891

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


  22 in total

1.  Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome.

Authors:  C Crosnier; C Driancourt; N Raynaud; S Dhorne-Pollet; N Pollet; O Bernard; M Hadchouel; M Meunier-Rotival
Journal:  Gastroenterology       Date:  1999-05       Impact factor: 22.682

2.  Features of Alagille syndrome in 92 patients: frequency and relation to prognosis.

Authors:  K M Emerick; E B Rand; E Goldmuntz; I D Krantz; N B Spinner; D A Piccoli
Journal:  Hepatology       Date:  1999-03       Impact factor: 17.425

3.  Mutations in the human Jagged1 gene are responsible for Alagille syndrome.

Authors:  T Oda; A G Elkahloun; B L Pike; K Okajima; I D Krantz; A Genin; D A Piccoli; P S Meltzer; N B Spinner; F S Collins; S C Chandrasekharappa
Journal:  Nat Genet       Date:  1997-07       Impact factor: 38.330

4.  Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1.

Authors:  L Li; I D Krantz; Y Deng; A Genin; A B Banta; C C Collins; M Qi; B J Trask; W L Kuo; J Cochran; T Costa; M E Pierpont; E B Rand; D A Piccoli; L Hood; N B Spinner
Journal:  Nat Genet       Date:  1997-07       Impact factor: 38.330

5.  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 6.  Alagille syndrome.

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

7.  Familial Tetralogy of Fallot caused by mutation in the jagged1 gene.

Authors:  Z A Eldadah; A Hamosh; N J Biery; R A Montgomery; M Duke; R Elkins; H C Dietz
Journal:  Hum Mol Genet       Date:  2001-01-15       Impact factor: 6.150

Review 8.  Alagille syndrome. The widening spectrum of arteriohepatic dysplasia.

Authors:  C Crosnier; P Lykavieris; M Meunier-Rotival; M Hadchouel
Journal:  Clin Liver Dis       Date:  2000-11       Impact factor: 6.126

Review 9.  Jagged1 mutations in alagille syndrome.

Authors:  N B Spinner; R P Colliton; C Crosnier; I D Krantz; M Hadchouel; M Meunier-Rotival
Journal:  Hum Mutat       Date:  2001       Impact factor: 4.878

10.  Skeletal anomalies and deformities in patients with deletions of 22q11.

Authors:  J E Ming; D M McDonald-McGinn; T E Megerian; D A Driscoll; E R Elias; B M Russell; M Irons; B S Emanuel; R I Markowitz; E H Zackai
Journal:  Am J Med Genet       Date:  1997-10-17
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  44 in total

1.  Pathologic lower extremity fractures in children with Alagille syndrome.

Authors:  Christina B Bales; Binita M Kamath; Pedro S Munoz; Alexander Nguyen; David A Piccoli; Nancy B Spinner; David Horn; Justine Shults; Mary B Leonard; Adda Grimberg; Kathleen M Loomes
Journal:  J Pediatr Gastroenterol Nutr       Date:  2010-07       Impact factor: 2.839

Review 2.  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

3.  Alagille syndrome in a Vietnamese cohort: mutation analysis and assessment of facial features.

Authors:  Henry C Lin; Phuc Le Hoang; Anne Hutchinson; Grace Chao; Jennifer Gerfen; Kathleen M Loomes; Ian Krantz; Binita M Kamath; Nancy B Spinner
Journal:  Am J Med Genet A       Date:  2012-04-09       Impact factor: 2.802

4.  Jagged1 (JAG1) mutations in patients with tetralogy of Fallot or pulmonic stenosis.

Authors:  Robert C Bauer; Ayanna O Laney; Rosemarie Smith; Jennifer Gerfen; Jennifer J D Morrissette; Stacy Woyciechowski; Jennifer Garbarini; Kathleen M Loomes; Ian D Krantz; Zsolt Urban; Bruce D Gelb; Elizabeth Goldmuntz; Nancy B Spinner
Journal:  Hum Mutat       Date:  2010-05       Impact factor: 4.878

Review 5.  Notch signaling in human development and disease.

Authors:  Andrea L Penton; Laura D Leonard; Nancy B Spinner
Journal:  Semin Cell Dev Biol       Date:  2012-01-28       Impact factor: 7.727

Review 6.  Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

Authors:  Mary Ella Pierpont; Martina Brueckner; Wendy K Chung; Vidu Garg; Ronald V Lacro; Amy L McGuire; Seema Mital; James R Priest; William T Pu; Amy Roberts; Stephanie M Ware; Bruce D Gelb; Mark W Russell
Journal:  Circulation       Date:  2018-11-20       Impact factor: 29.690

7.  New Genetic Insights into Congenital Heart Disease.

Authors:  Stephanie M Ware; John Lynn Jefferies
Journal:  J Clin Exp Cardiolog       Date:  2012-06-15

8.  NOTCH2 mutations in Alagille syndrome.

Authors:  Binita Maya Kamath; Robert C Bauer; Kathleen M Loomes; Grace Chao; Jennifer Gerfen; Anne Hutchinson; Winita Hardikar; Gideon Hirschfield; Paloma Jara; Ian D Krantz; Pablo Lapunzina; Laura Leonard; Simon Ling; Vicky Lee Ng; Phuc Le Hoang; David A Piccoli; Nancy Bettina Spinner
Journal:  J Med Genet       Date:  2011-12-29       Impact factor: 6.318

9.  Clinical Features and Genetic Analysis of Pediatric Patients with Alagille Syndrome Presenting Initially with Liver Function Abnormalities.

Authors:  Yan Liu; Hong Wang; Chen Dong; Jie-Xiong Feng; Zhi-Hua Huang
Journal:  Curr Med Sci       Date:  2018-04-30

Review 10.  Congenital cholestatic syndromes: what happens when children grow up?

Authors:  S C Ling
Journal:  Can J Gastroenterol       Date:  2007-11       Impact factor: 3.522

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