Literature DB >> 2162657

Sturge-Weber and Klippel-Trenaunay syndromes with absence of inferior vena cava.

G Stewart1, G Farmer.   

Abstract

A baby girl born at 33 weeks' gestation weighing 2250 g presented with Sturge-Weber syndrome, features of the Klippel-Trenaunay syndrome, and absence of the inferior vena cava. We suggest that aplasia of the vena cava may be a feature of Klippel-Trenaunay syndrome when the capillary malformation affects the trunk.

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Year:  1990        PMID： 2162657      PMCID： PMC1792157          DOI： 10.1136/adc.65.5.546

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


  3 in total

1.  Klippel and Trénaunay's syndrome. 768 operated cases.

Authors:  M Servelle
Journal:  Ann Surg       Date:  1985-03       Impact factor: 12.969

2.  The Klippel-Trenaunay syndrome: clinical, radiological and haemodynamic features and management.

Authors:  P A Baskerville; J S Ackroyd; M Lea Thomas; N L Browse
Journal:  Br J Surg       Date:  1985-03       Impact factor: 6.939

3.  Klippel-Trenaunay and Sturge-Weber syndromes with renal hemangioma and double inferior vena cava.

Authors:  D Schofield; G S Zaatari; B B Gay
Journal:  J Urol       Date:  1986-08       Impact factor: 7.450
  3 in total
  2 in total

1.  Focal venous hypertension as a pathophysiologic mechanism for tissue hypertrophy, port-wine stains, the Sturge-Weber syndrome, and related disorders: proof of concept with novel hypothesis for underlying etiological cause (an American Ophthalmological Society thesis).

Authors:  Cameron F Parsa
Journal:  Trans Am Ophthalmol Soc       Date:  2013-09

2.  A rare paediatric case of Klippel-Trenaunay-Weber syndrome.

Authors:  Jennifer A Howes; Guru Setty; Arif Khan; Nahin Hussain
Journal:  J Pediatr Neurosci       Date:  2015 Jan-Mar
  2 in total

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