Literature DB >> 6873941

X-linked dominant inherited diseases with lethality in hemizygous males.

R Wettke-Schäfer, G Kantner.   

Abstract

X-linked dominant inheritance with lethality in hemizygous males is a rare mode of inheritance. The three best-known disorders which seem to be inherited in this way, are incontinentia pigmenti (IP) Bloch-Sulzberger, oral-facial-digital I (OFD I) syndrome, and focal dermal hypoplasia (FDH syndrome, Goltz syndrome). It is the purpose of this article to give a review of the clinical and genetic aspects of the above-mentioned diseases and to add those disorders in which this mode of inheritance is discussed. These disorders are: X-linked chondrodysplasia punctata (CP), cervico-oculo-acusticus syndrome (Wildervanck syndrome, COA), congenital cataract with microcornea or slight microphthalmia, muscular dystrophy--hemizygous lethal, partial lipodystrophy with lipatrophic diabetes and hyperlipidemia, Aicardi syndrome, coxo-auricular syndrome, and Johanson-Blizzard syndrome. OTC deficiency is included in the study, although there is no lethality in utero, only in the neonatal period. A critical evaluation of the current literature is carried out.

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Year:  1983        PMID: 6873941     DOI: 10.1007/bf00289472

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  182 in total

1.  HEREDITARY CATARACTS AND MICROPHTHALMIA.

Authors:  J A CAPELLA; H E KAUFMAN; F J LILL
Journal:  Am J Ophthalmol       Date:  1963-09       Impact factor: 5.258

2.  Hyperammonaemia due to ornithine transcarbamylase deficiency.

Authors:  I J Hopkins; J F Connelly; A G Dawson; F J Hird; T G Maddison
Journal:  Arch Dis Child       Date:  1969-04       Impact factor: 3.791

3.  Reye's syndrome due to a novel protein-tolerant variant of ornithine-transcarbamylase deficiency.

Authors:  M M Thaler; N J Hoogenraad; M Boswell
Journal:  Lancet       Date:  1974-08-24       Impact factor: 79.321

4.  Hyperammonemia due to a defect in hepatic ornithine transcarbamylase.

Authors:  P Sunshine; J E Lindenbaum; H L Levy; J M Freeman
Journal:  Pediatrics       Date:  1972-07       Impact factor: 7.124

5.  Heterogeneity of Chondrodysplasia punctata.

Authors:  J W Spranger; J M Opitz; U Bidder
Journal:  Humangenetik       Date:  1971

6.  The Aicardi syndrome in a 47, XXY male.

Authors:  I J Hopkins; I Humphrey; C G Keith; M Susman; G C Webb; E K Turner
Journal:  Aust Paediatr J       Date:  1979-12

7.  Agenesis of the corpus callosum, infantile spasms, ocular anomalies (Aicardi's syndrome). Clinical and pathologic findings.

Authors:  J G de Jong; J W Delleman; M Houben; W A Manschot; A de Minjer; J Mol; J L Slooff
Journal:  Neurology       Date:  1976-12       Impact factor: 9.910

8.  Carrier detection in ornithine transcarbamylase deficiency.

Authors:  J T Hokanson; W E O'Brien; J Idemoto; I A Schafer
Journal:  J Pediatr       Date:  1978-07       Impact factor: 4.406

9.  Melnick-Needles syndrome: indication for an autosomal recessive form.

Authors:  B ter Haar; B Hamel; J Hendriks; J de Jager
Journal:  Am J Med Genet       Date:  1982-12

10.  [X-linked dominant chondrodysplasia punctata (author's transl)].

Authors:  R Happle
Journal:  Monatsschr Kinderheilkd       Date:  1980-04
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  27 in total

1.  MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin.

Authors:  R Trappe; F Laccone; J Cobilanschi; M Meins; P Huppke; F Hanefeld; W Engel
Journal:  Am J Hum Genet       Date:  2001-04-17       Impact factor: 11.025

2.  High male:female ratio of germ-line mutations: an alternative explanation for postulated gestational lethality in males in X-linked dominant disorders.

Authors:  G H Thomas
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

Review 3.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

Review 4.  The genetic basis of incomitant strabismus: consolidation of the current knowledge of the genetic foundations of disease.

Authors:  Carolyn P Graeber; David G Hunter; Elizabeth C Engle
Journal:  Semin Ophthalmol       Date:  2013 Sep-Nov       Impact factor: 1.975

5.  Aicardi syndrome associated with autosomal genomic imbalance: coincidence or evidence for autosomal inheritance with sex-limited expression?

Authors:  P Prontera; A Bartocci; V Ottaviani; I Isidori; D Rogaia; C Ardisia; G Guercini; A Mencarelli; E Donti
Journal:  Mol Syndromol       Date:  2013-04-11

6.  Selection against lethal alleles in females heterozygous for incontinentia pigmenti.

Authors:  B R Migeon; J Axelman; S Jan de Beur; D Valle; G A Mitchell; K N Rosenbaum
Journal:  Am J Hum Genet       Date:  1989-01       Impact factor: 11.025

Review 7.  Lyonization and the lines of Blaschko.

Authors:  R Happle
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

8.  A probable sex difference in mutation rates in ornithine transcarbamylase deficiency.

Authors:  C Bonaïti-Pellié; A Pelet; H Ogier; J R Nelson; C Largillière; J Berthelot; J M Saudubray; A Munnich
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

9.  Carrier detection in a partially dominant X-linked disease: ornithine transcarbamylase deficiency.

Authors:  A Pelet; A Rotig; C Bonaïti-Pellié; D Rabier; V Cormier; E Toumas; D Hentzen; J M Saudubray; A Munnich
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

10.  Neuroimaging aspects of Aicardi syndrome.

Authors:  Bobbi Hopkins; V Reid Sutton; Richard Alan Lewis; Ignatia Van den Veyver; Gary Clark
Journal:  Am J Med Genet A       Date:  2008-11-15       Impact factor: 2.802

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