J 2000

Smith-Lemli-Opitz syndrome:Molecular-genetic analysis of ten families

KOZÁK, Libor, Hana FRANCOVÁ, Eva HRABINCOVÁ, Dagmar PROCHÁZKOVÁ, V. JUTTNEROVÁ et. al.

Basic information

Original name

Smith-Lemli-Opitz syndrome:Molecular-genetic analysis of ten families

Authors

KOZÁK, Libor, Hana FRANCOVÁ, Eva HRABINCOVÁ, Dagmar PROCHÁZKOVÁ, V. JUTTNEROVÁ, V. BZDÚCH and P. ŠIMEK

Edition

JOURNAL OF Inherited Metabolic Disease, Lancaster (United Kingdom), SSIEM and Kluwer Academic Publisher, 2000, 0141-8955

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

Genetics and molecular biology

Country of publisher

United Kingdom of Great Britain and Northern Ireland

Confidentiality degree

není předmětem státního či obchodního tajemství

Impact factor

Impact factor: 1.307

Organization unit

Faculty of Science

Keywords in English

Smith-Lemli-Opitz syndrome; SLOS; 7-dehydrocholesterol reductase; DHCR7; Czech; Slovak

Tags

Změněno: 2/2/2001 15:11, Mgr. Eva Hrabincová

Abstract

V originále

Smith-Lemli-Opitz syndrome (SLOS; McKusick 270400) is an autosomal recessive inherited metabolic-malformation disorder caused by deficient activity of 7-dehydrocholesterol reductase (DHCR7, E.C. 1.3.1.21), which catalyses the final step in the cholesterol-biosynthesis pathway. The clinical picture is characterized by a combination of congenital anomalies: microcephaly, hypotonia, incomplete development of the male genitalia, polydactyly, syndactyly of toes 2 and 3, cleft palate, heart and kidney malformations, failure to thrive and severe mental and growth retardation (Smith et al 1964). A decrease of plasma cholesterol and the accumulation of its precursor 7-dehydrocholesterol (7-DHC) is the biochemical hallmark in SLOS patients (Tint et al 1994). Cloning and sequncing of DHCR7 cDNA (Moebius et al 1998) and characterization of the human DHCR7 gene (Fitzky et al 1998) enabled investigation of defects of this gene at the DNA level. Several mutations have been described (Wassif et al 1998; Waterham et al 1998). Here we report the results of molecular analysis of the DHCR7 gene in 10 unrelated families with Smith-Lemli-Opitz syndrome. Results of mutation analyses are presented and compared with the clinical and biochemical data.