Literature DB >> 3236362

Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.

D Donnai1, A P Read, C McKeown, T Andrews.   

Abstract

We describe three patients with the cutaneous manifestations of hypomelanosis of Ito. Two, with unusual abnormalities of their toes, had a mixture of diploid and triploid cells in cultured skin fibroblasts. The published clinical descriptions of hypomelanosis of Ito and diploid-triploid mosaicism are reviewed. Chromosome heteromorphisms, HLA types, and DNA fingerprints were studied in an attempt to elucidate the origin of the disease in our patients. We conclude that hypomelanosis of Ito is a manifestation of a heterogeneous group of disorders, the common factor being the presence of two genetically different cell lines. It can result from chromosomal mosaicism or chimerism, from a postzygotic mutation, or from X inactivation. The risk of recurrence is negligible if the proband is a male; if the proband is female the risk is also low but an X linked mutation must be considered.

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Year:  1988        PMID: 3236362      PMCID: PMC1051608          DOI: 10.1136/jmg.25.12.809

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


  33 in total

1.  [Triploidy in the child. I. Study of phenotype. An observation of triploidy with mosaicism 46, XX/69, XXY].

Authors:  M David; A Chambon; C Laurent; H Plauchu; D Lindner; A Rouchon; E de Peretti; J Genoud; M Jeune
Journal:  Pediatrie       Date:  1975 Apr-May

2.  A diploid-triploid human mosaic with cytogenetic evidence of double fertilization.

Authors:  G Dewald; M N Alvarez; M D Cloutier; P P Kelalis; H Gordon
Journal:  Clin Genet       Date:  1975-08       Impact factor: 4.438

Review 3.  Triploidy in man. Cytogenetical and clinical aspects.

Authors:  E Niebuhr
Journal:  Humangenetik       Date:  1974-02-21

4.  Hypomelanosis of Ito ("incontinentia pigmenti achromians"). Report of three cases and review of the literature.

Authors:  J E Jelinek; R S Bart; S M Schiff
Journal:  Arch Dermatol       Date:  1973-04

5.  Comparison between mice chimaeric and heterozygous for the X-linked gene tabby.

Authors:  A McLaren; I K Gauld; P Bowman
Journal:  Nature       Date:  1973-01-19       Impact factor: 49.962

Review 6.  The lines of Blaschko: a review and reconsideration: Observations of the cause of certain unusual linear conditions of the skin.

Authors:  R Jackson
Journal:  Br J Dermatol       Date:  1976-10       Impact factor: 9.302

7.  Diploid-triploid mosaicism: delineation of the syndrome.

Authors:  A T Tharapel; R S Wilroy; P R Martens; J M Holbert; R L Summitt
Journal:  Ann Genet       Date:  1983

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

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

9.  Hypomelanosis of Ito (incontinentia pigmenti achromians): a neurocutaneous syndrome.

Authors:  M F Schwartz; N B Esterly; D F Fretzin; E Pergament; I H Rozenfeld
Journal:  J Pediatr       Date:  1977-02       Impact factor: 4.406

10.  Aberrant melanoblast migration associated with trisomy 18 mosaicism.

Authors:  J Chemke; S Rappaport; R Etrog
Journal:  J Med Genet       Date:  1983-04       Impact factor: 6.318

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  25 in total

1.  "Cutis tricolor": congenital hyper- and hypopigmented macules associated with a sporadic multisystem birth defect: an unusual example of twin spotting?

Authors:  R Happle; G Barbi; D Eckert; I Kennerknecht
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

2.  Diagnostic evaluation for asymmetry: consider genetic mosaicism.

Authors:  Koen Devriendt; Jean-Pierre Fryns
Journal:  Eur J Pediatr       Date:  2004-10       Impact factor: 3.183

3.  Anterior segment dysgenesis in mosaic Turner syndrome.

Authors:  I C Lloyd; P M Haigh; J Clayton-Smith; P Clayton; D A Price; A E Ridgway; D Donnai
Journal:  Br J Ophthalmol       Date:  1997-08       Impact factor: 4.638

Review 4.  [Skin and teeth].

Authors:  J Heinlin; N Heinlin; J Steinbauer; M Landthaler; S Karrer
Journal:  Hautarzt       Date:  2009-07       Impact factor: 0.751

5.  46,XX/69,XXX diploid-triploid mixoploidy with hypothyroidism and precocious puberty.

Authors:  I E Järvelä; M K Salo; P Santavuori; R K Salonen
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

Review 6.  Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

Authors:  E Hatchwell
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

Review 7.  Dysmorphic disorders--an overview.

Authors:  D Donnai
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

Review 8.  Heterogeneous seizure manifestations in Hypomelanosis of Ito: report of four new cases and review of the literature.

Authors:  Komi Assogba; Edoardo Ferlazzo; Pasquale Striano; Tiziana Calarese; Nathalie Villeneuve; Ivan Ivanov; Placido Bramanti; Edoardo Sessa; Iliana Pacheva; Pierre Genton
Journal:  Neurol Sci       Date:  2009-11-10       Impact factor: 3.307

Review 9.  Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.

Authors:  I T Thomas; J L Frias; E S Cantu; C Z Lafer; D B Flannery; J G Graham
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

10.  Pigmentary mosaicism: an update.

Authors:  Rajoo Thapa
Journal:  Indian J Dermatol       Date:  2008       Impact factor: 1.494

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