Literature DB >> 2831368

Lethal acrodysgenital dwarfism: a severe lethal condition resembling Smith-Lemli-Opitz syndrome.

M L Merrer1, M L Briard, S Girard, N Mulliez, C Moraine, M C Imbert.   

Abstract

We report eight cases of a lethal association of failure to thrive, facial dysmorphism, ambiguous genitalia, syndactyly, postaxial polydactyly, and internal developmental anomalies (Hirschsprung's disease, cardiac and renal malformation). This syndrome is likely to be autosomal recessive and resembles Smith-Lemli-Opitz (SLO) syndrome. However, the lethality, the common occurrence of polydactyly, and the sexual ambiguity distinguishes this condition from SLO syndrome. A review of published reports supports the separate classification of this syndrome for which we propose the name lethal acrodysgenital dwarfism.

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Year:  1988        PMID: 2831368      PMCID: PMC1015449          DOI: 10.1136/jmg.25.2.88

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  29 in total

1.  A FAMILIAL SYNDROME OF FACIAL AND SKELETAL ANOMALIES ASSOCIATED WITH GENITAL ABNORMALITY IN THE MALE AND NORAML GENITALS IN THE FEMALE: ANOTHER CAUSE OF MALE PSEUDOHERMAPHRODITISM.

Authors:  L PINSKY; A M DIGEORGE
Journal:  J Pediatr       Date:  1965-06       Impact factor: 4.406

2.  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

3.  [Smith-Lemli-Opitz dwarfism. Report of four cases. Review of the literature].

Authors:  J Cruveiller; S Msika; J Lafourcade
Journal:  Ann Pediatr (Paris)       Date:  1977-12

4.  [An unrecognized etiology of sexual ambiguity: Smith-Lemli-Opitz syndrome or a new entity?].

Authors:  M Le Merrer; M L Briard; M L Chauvet
Journal:  J Genet Hum       Date:  1987-05

5.  Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance.

Authors:  L Dallaire
Journal:  J Med Genet       Date:  1969-06       Impact factor: 6.318

6.  Hereditary syndrome of imperforate anus with hand, foot, and ear anomalies.

Authors:  P L Townes; E R Brocks
Journal:  J Pediatr       Date:  1972-08       Impact factor: 4.406

7.  Smith-Lemli-Opitz syndrome. Case report.

Authors:  R H Ruvalcaba; A Reichert; D W Smith
Journal:  Arch Dis Child       Date:  1968-10       Impact factor: 3.791

8.  Micrognathia, polydactyly, and cleft palate.

Authors:  R B Lowry; J R Miller; J R MacLean
Journal:  J Pediatr       Date:  1968-06       Impact factor: 4.406

9.  Cataracts in a girl with features of the Smith-Lemli-Opitz syndrome.

Authors:  S C Finley; W H Finley; D B Monsky
Journal:  J Pediatr       Date:  1969-10       Impact factor: 4.406

10.  A syndrome characterized by mental retardation, short stature, craniofacial dysplasia, and genital anomalies occurring in siblings.

Authors:  H R Blair; J K Martin
Journal:  J Pediatr       Date:  1966-09       Impact factor: 4.406

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  8 in total

1.  A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): potential mapping of one disease locus.

Authors:  A Bottani; Y G Xie; F Binkert; A Schinzel
Journal:  Hum Genet       Date:  1991-10       Impact factor: 4.132

Review 2.  The Smith-Lemli-Opitz syndrome.

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

3.  Smith-Lemli-Opitz syndrome. II: A disorder of the fetal adrenals?

Authors:  P A McKeever; I D Young
Journal:  J Med Genet       Date:  1990-07       Impact factor: 6.318

4.  MRI in Smith-Lemli-Opitz syndrome type I.

Authors:  G Trasimeni; C Di Biasi; M Iannilli; L Orlandi; B Boscherini; R Balducci; G F Gualdi
Journal:  Childs Nerv Syst       Date:  1997-01       Impact factor: 1.475

5.  Stringent delineation of Pallister-Hall syndrome in two long surviving patients: importance of radiological anomalies of the hands.

Authors:  A Verloes; A David; L Ngô; A Bottani
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

6.  Smith-Lemli-Opitz syndrome type II: report of a case with additional radiographic findings.

Authors:  T E Herman; M J Siegel; B C Lee; S B Dowton
Journal:  Pediatr Radiol       Date:  1993

7.  Abnormal cholesterol biosynthesis in the Smith-Lemli-Opitz and the lethal acrodysgenital syndromes.

Authors:  V Cormier-Daire; C Wolf; A Munnich; M Le Merrer; A Nivelon; D Bonneau; H Journel; F Fellmann; F Chevy; C Roux
Journal:  Eur J Pediatr       Date:  1996-08       Impact factor: 3.183

Review 8.  Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study.

Authors:  A Verloes; S Aymé; D Gambarelli; M Gonzales; M Le Merrer; N Mulliez; N Philip; J Roume
Journal:  J Med Genet       Date:  1991-05       Impact factor: 6.318

  8 in total

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