Literature DB >> 15834578

Surgical implications of the Smith-Lemli-Opitz syndrome.

R J Craigie1, M Ba'ath, A Fryer, C Baillie.   

Abstract

Smith-Lemli-Opitz syndrome (SLOS) is a syndrome of rare multiple congenital anomalies/mental retardation associated with low plasma cholesterol levels. Prior to receiving the diagnosis of SLOS, affected children may present as a neonatal surgical emergency with ambiguous genitalia, Hirschsprung's disease, and pyloric stenosis. We present two fatal cases of SLOS with near-total Hirschsprung's disease; the surgical, anaesthetic, and medical aspects of the cases are discussed, and a literature review is presented.

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Year:  2005        PMID: 15834578     DOI: 10.1007/s00383-005-1415-8

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  17 in total

1.  A NEWLY RECOGNIZED SYNDROME OF MULTIPLE CONGENITAL ANOMALIES.

Authors:  D W SMITH; L LEMLI; J M OPITZ
Journal:  J Pediatr       Date:  1964-02       Impact factor: 4.406

Review 2.  Congenital abnormalities of body patterning: embryology revisited.

Authors:  Frances R Goodman
Journal:  Lancet       Date:  2003-08-23       Impact factor: 79.321

Review 3.  The Smith-Lemli-Opitz syndrome.

Authors:  R I Kelley; R C Hennekam
Journal:  J Med Genet       Date:  2000-05       Impact factor: 6.318

4.  Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality.

Authors:  C J Curry; J C Carey; J S Holland; D Chopra; R Fineman; M Golabi; S Sherman; R A Pagon; J Allanson; S Shulman
Journal:  Am J Med Genet       Date:  1987-01

5.  Limb, genital, CNS, and facial malformations result from gene/environment-induced cholesterol deficiency: further evidence for a link to sonic hedgehog.

Authors:  L Lanoue; D B Dehart; M E Hinsdale; N Maeda; G S Tint; K K Sulik
Journal:  Am J Med Genet       Date:  1997-11-28

6.  Smith-Lemli-Opitz syndrome and Hirschsprung disease.

Authors:  A Lipson; A Hayes
Journal:  J Pediatr       Date:  1984-07       Impact factor: 4.406

7.  Smith-Lemli-Opitz syndrome associated with Hirschsprung disease, 46,XY female karyotype, and total anomalous pulmonary venous drainage.

Authors:  E H Kim; W C Boutwell
Journal:  J Pediatr       Date:  1985-05       Impact factor: 4.406

8.  Intestinal aganglionosis in the Smith-Lemli-Opitz syndrome.

Authors:  J Zizka; J Maresová; Z Kerekes; Z Nozicka; V Jüttnerová; P Balícek
Journal:  Acta Paediatr Scand       Date:  1983-01

9.  Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations.

Authors:  M Witsch-Baumgartner; E Ciara; J Löffler; H J Menzel; U Seedorf; J Burn; G Gillessen-Kaesbach; G F Hoffmann; B U Fitzky; H Mundy; P Clayton; R I Kelley; M Krajewska-Walasek; G Utermann
Journal:  Eur J Hum Genet       Date:  2001-01       Impact factor: 4.246

10.  Abnormal cholesterol biosynthesis as in Smith-Lemli-Opitz syndrome disrupts normal skeletal development in the rat.

Authors:  M Kolf-Clauw; F Chevy; C Ponsart
Journal:  J Lab Clin Med       Date:  1998-03
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  1 in total

Review 1.  [Syndromic Hirschsprung′s disease and its mode of inheritance].

Authors:  Jing-Ru Zhang; Zhi-Bo Zhang
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2018-05
  1 in total

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