Literature DB >> 3732319

Bronze baby syndrome, biliary hypoplasia, incomplete Beckwith-Wiedemann syndrome and partial trisomy 11.

J K Wales, V Walker, I E Moore, P T Clayton.   

Abstract

A premature infant with duplication of material from chromosome 11 and some features of the Beckwith-Wiedemann syndrome developed the bronze baby syndrome when exposed to phototherapy. He subsequently developed hepatocellular dysfunction and died aged 5 weeks. Post mortem examination revealed striking hypoplasia of intralobular bile ducts but little inflammatory change or necrosis in the liver.

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Year:  1986        PMID： 3732319     DOI： 10.1007/bf00441878

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


  6 in total

1.  A complication of phototherapy in the newborn: the "bronze baby".

Authors:  R K Sharma; G Ente; P J Collipp; V T Maddaiah; I Rezvani
Journal:  Clin Pediatr (Phila)       Date:  1973-04       Impact factor: 1.168

2.  The "bronze" baby syndrome: a complication of phototherapy.

Authors:  A E Kopelman; R S Brown; G B Odell
Journal:  J Pediatr       Date:  1972-09       Impact factor: 4.406

3.  Bronze baby syndrome: a new porphyrin-related disorder.

Authors:  F F Rubaltelli; G Jori; E Reddi
Journal:  Pediatr Res       Date:  1983-05       Impact factor: 3.756

4.  The "bronze baby" syndrome: postmortem data.

Authors:  C F Clark; S Torii; Y Hamamoto; H Kaito
Journal:  J Pediatr       Date:  1976-03       Impact factor: 4.406

5.  Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome.

Authors:  M Waziri; S R Patil; J W Hanson; J A Bartley
Journal:  J Pediatr       Date:  1983-06       Impact factor: 4.406

6.  The bronze baby syndrome.

Authors:  K L Tan; E Jacob
Journal:  Acta Paediatr Scand       Date:  1982-05
  6 in total
  7 in total

Review 1.  The side effects of phototherapy for neonatal jaundice: what do we know? What should we do?

Authors:  Tao Xiong; Yi Qu; Stephanie Cambier; Dezhi Mu
Journal:  Eur J Pediatr       Date:  2011-04-01       Impact factor: 3.183

2.  Genomic imprinting and the Beckwith-Wiedemann syndrome.

Authors:  K W Brown; J C Williams; N J Maitland; M G Mott
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

3.  Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females.

Authors:  C Moutou; C Junien; I Henry; C Bonaïti-Pellié
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

Review 4.  Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome.

Authors:  A Slavotinek; L Gaunt; D Donnai
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318

Review 5.  Structural alteration of the insulin-like growth factor II-gene in Wilms tumour.

Authors:  J C Irminger; E J Schoenle; J Briner; R E Humbel
Journal:  Eur J Pediatr       Date:  1989-06       Impact factor: 3.183

6.  Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5).

Authors:  N Tommerup; C A Brandt; S Pedersen; L Bolund; J Kamper
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

7.  Insulin-like growth factor 2 cannot be linked to a familial form of Beckwith-Wiedemann syndrome.

Authors:  A Nyström; F Hedborg; R Ohlsson
Journal:  Eur J Pediatr       Date:  1994-08       Impact factor: 3.183
  7 in total

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