Literature DB >> 1937482

A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): potential mapping of one disease locus.

A Bottani1, Y G Xie, F Binkert, A Schinzel.   

Abstract

A mentally retarded boy with discrete physical findings, Hirschsprung disease (HD) and a microdeletion of 13q,del(13)(q32.3q33.2) is described. Band 13q33.1 was consistently missing in all cells. There have been, to date, 4 published cases of deletions involving the long arm of chromosome 13 associated with HD: the interstitial deletion reported here is much smaller than, and it partially overlaps with, the previously reported deletions; it could be helpful for mapping one of the genes involved in this disease.

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Year:  1991        PMID: 1937482     DOI: 10.1007/bf00201741

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  23 in total

1.  A genetic study of Hirschsprung disease.

Authors:  J A Badner; W K Sieber; K L Garver; A Chakravarti
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025

2.  Hirschsprung's disease and Waardenburg's syndrome.

Authors:  D Branski; N R Dennis; J M Neale; L J Brooks
Journal:  Pediatrics       Date:  1979-05       Impact factor: 7.124

3.  Hirschsprung disease: etiologic implications of unsuccessful prenatal diagnosis.

Authors:  A L Jarmas; D D Weaver; L M Padilla; E Stecker; H A Bender
Journal:  Am J Med Genet       Date:  1983-10

4.  Corneal opacities--a diagnostic feature of the trisomy 8 mosaic syndrome.

Authors:  M Frangoulis; D Taylor
Journal:  Br J Ophthalmol       Date:  1983-09       Impact factor: 4.638

5.  The association of Waardenburg syndrome and Hirschsprung megacolon.

Authors:  G S Omenn; V A McKusick
Journal:  Am J Med Genet       Date:  1979

6.  Multiple congenital defects associated with trisomy for long arm of No. 4.

Authors:  M Issa; A M Potter; C E Blank
Journal:  J Med Genet       Date:  1976-08       Impact factor: 6.318

7.  "Partial trisomy 22 and 11" due to a paternal 11;22 translocation associated with Hirschsprung disease.

Authors:  B Beedgen; W Nützenadel; U Querfeld; P Weiss-Wichert
Journal:  Eur J Pediatr       Date:  1986-08       Impact factor: 3.183

8.  Brief clinical report: an infant with duplication of 17q21 lead to 17qter.

Authors:  J U Gallien; R L Neu; R J Wynn; N Steinberg-Warren; R M Bannerman
Journal:  Am J Med Genet       Date:  1981

9.  Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and delection 10q.

Authors:  L M Larson; W A Wasdahl; J H Saumur; M L Coleman; J G Hall; C R Dolan; C J Schutta
Journal:  Clin Genet       Date:  1982-03       Impact factor: 4.438

Review 10.  Lethal acrodysgenital dwarfism: a severe lethal condition resembling Smith-Lemli-Opitz syndrome.

Authors:  M L Merrer; M L Briard; S Girard; N Mulliez; C Moraine; M C Imbert
Journal:  J Med Genet       Date:  1988-02       Impact factor: 6.318

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  13 in total

Review 1.  Hirschsprung disease, associated syndromes, and genetics: a review.

Authors:  J Amiel; S Lyonnet
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

2.  Band-specific localization of the microsatellite at D13S71 by microdissection and enzymatic amplification.

Authors:  H Spielvogel; H C Hennies; U Claussen; S S Washington; A Chakravarti; A Reis
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

Review 3.  Mutations of the endothelin-B receptor and endothelin-3 genes in Hirschsprung's disease.

Authors:  T Kusafuka; P Puri
Journal:  Pediatr Surg Int       Date:  1997       Impact factor: 1.827

Review 4.  Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.

Authors:  N Tommerup
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

Review 5.  Hirschsprung's disease: genetic mutations in mice and men.

Authors:  K Robertson; I Mason; S Hall
Journal:  Gut       Date:  1997-10       Impact factor: 23.059

Review 6.  Chromosomal and related Mendelian syndromes associated with Hirschsprung's disease.

Authors:  S W Moore
Journal:  Pediatr Surg Int       Date:  2012-09-23       Impact factor: 1.827

7.  The 13q- syndrome: the molecular definition of a critical deletion region in band 13q32.

Authors:  S Brown; J Russo; D Chitayat; D Warburton
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

8.  Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.

Authors:  P Edery; A Pelet; L M Mulligan; L Abel; T Attié; E Dow; D Bonneau; A David; W Flintoff; D Jan
Journal:  J Med Genet       Date:  1994-08       Impact factor: 6.318

9.  Umbilical cord ulceration in association with intestinal atresia in a child with deletion 13q and Hirschsprung's disease.

Authors:  T Y Khong; W D Ford; E A Haan
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1994-11       Impact factor: 5.747

Review 10.  Hirschsprung's disease associated with a deletion of chromosome 10 (q11.2q21.2): a further link with the neurocristopathies?

Authors:  M S Fewtrell; P K Tam; A H Thomson; M Fitchett; J Currie; S M Huson; L M Mulligan
Journal:  J Med Genet       Date:  1994-04       Impact factor: 6.318

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