Literature DB >> 7097410

The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

R I Kelley, E H Zackai, B S Emanuel, M Kistenmacher, F Greenberg, H H Punnett.   

Abstract

We have seen three unrelated patients with the DiGeorge anomalad who also had the same deletion of chromosome 22 (pter leads to qll). In each, the remaining long arm material (qll leads to qter) was translocated to a different autosome. Our patients and a review of the literature, including a recent report of a family having four infants with the DiGeorge anomalad and the same deletion of chromosome 22 (de la Chapelle et al: Hum Genet 57:253, 1981), make a strong argument for at least some cases of the DiGeorge anomalad arising from a deletion of the pericentromeric region of chromosome 22.

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Year:  1982        PMID: 7097410     DOI: 10.1016/s0022-3476(82)80116-9

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  56 in total

1.  Defective growth hormone secretion and hypogonadism in the new syndrome of congenital hypoparathyroidism, growth failure and dysmorphic features.

Authors:  A T Soliman; A Darwish; I alSalmi; M Asfour
Journal:  Indian J Pediatr       Date:  1996 Sep-Oct       Impact factor: 1.967

2.  A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

Authors:  D A Driscoll; M L Budarf; B S Emanuel
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

3.  A prospective cytogenetic study of 36 cases of DiGeorge syndrome.

Authors:  D I Wilson; I E Cross; J A Goodship; J Brown; P J Scambler; H H Bain; J F Taylor; K Walsh; A Bankier; J Burn
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

Review 4.  Molecular genetics of mineral metabolic disorders.

Authors:  R V Thakker
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

Review 5.  Gene mapping of mineral metabolic disorders.

Authors:  R V Thakker; K E Davies; J L O'Riordan
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

6.  Two sibs with Wolf-Hirschhorn and DiGeorge deletions resulting from an unbalanced chromosome rearrangement, 45,XX/XY, der(4)t(4;22) (p16.3;q11.2) mat,-22.

Authors:  K S Reddy; V Sulcova; B Siassi
Journal:  J Med Genet       Date:  1996-10       Impact factor: 6.318

7.  Practical guidelines for managing patients with 22q11.2 deletion syndrome.

Authors:  Anne S Bassett; Donna M McDonald-McGinn; Koen Devriendt; Maria Cristina Digilio; Paula Goldenberg; Alex Habel; Bruno Marino; Solveig Oskarsdottir; Nicole Philip; Kathleen Sullivan; Ann Swillen; Jacob Vorstman
Journal:  J Pediatr       Date:  2011-05-12       Impact factor: 4.406

8.  Deletion mapping of 22q11 in CATCH22 syndrome: identification of a second critical region.

Authors:  H Kurahashi; T Nakayama; Y Osugi; E Tsuda; M Masuno; K Imaizumi; T Kamiya; T Sano; S Okada; I Nishisho
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

9.  Aortic root dilatation associated with partial trisomy 7(q31.2----qter).

Authors:  K B Roche; J W Moore; R B Surana; B E Wilson
Journal:  Pediatr Cardiol       Date:  1989       Impact factor: 1.655

10.  Errors of morphogenesis and inborn errors of immunity 20 years after the discovery of DiGeorge anomaly.

Authors:  G R Burgio; A G Ugazio
Journal:  Eur J Pediatr       Date:  1985-05       Impact factor: 3.183

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