Literature DB >> 6364021

Roentgenologic findings of the hydrolethalus syndrome.

R Herva, U Seppänen.   

Abstract

The hydrolethalus syndrome is an autosomal recessive malformation syndrome which has been recently described in Finland. The name hydrolethalus refers to the main findings, namely polyhydramnios, hydrocephalus and lethality. The patients are either stillborn or die soon after birth. The typical roentgenologic findings are hypoplasia of the tibia associated with the anomalies of the respective bone ray, e.g. metatarsus primus varus atavisticus, hallux varus or hallux duplex varus and hydrocephalus with extreme micrognathia and a specific midline defect of the occipital bone.

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Year:  1984        PMID: 6364021     DOI: 10.1007/bf02386730

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  2 in total

1.  Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly".

Authors:  F C Fraser; A Lytwyn
Journal:  Am J Med Genet       Date:  1981

2.  The hydrolethalus syndrome: delineation of a "new", lethal malformation syndrome based on 28 patients.

Authors:  R Salonen; R Herva; R Norio
Journal:  Clin Genet       Date:  1981-05       Impact factor: 4.438

  2 in total
  2 in total

Review 1.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

2.  Hydrolethalus syndrome.

Authors:  R Salonen; R Herva
Journal:  J Med Genet       Date:  1990-12       Impact factor: 6.318

  2 in total

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