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Hereditary Acrokeratotic Poikiloderma

Hereditary Acrokeratotic Poikiloderma Abstract A dominantly inherited disorder has affected ten members of a family group. At present we recognize the following categories of clinical involvement: (1) vesicopustule formation which remains confined to the hands and feet (this process commences at from 1 to 3 months of age and resolves in late childhood); (2) widespread eczematous dermatitis somewhat resembling atopic eczema which starts between the ages of 3 and 6 months and completely resolves by 5 years of age; (3) the gradual appearance of a diffuse poikiloderma with striate and reticulate atrophy which spares only the face, scalp, and ears (the poikiloderma persists into adult life); and (4) the development of keratotic papules on the hands, feet, elbows, and knees, which first appear at varying times prior to 5 years of age and persist indefinitely. References 1. Costa OG: Acrokeratoelastoidosis . Derm Latin Amer 1:189-193, 1966. 2. Rook A, David R, Stevanovic D: Poikiloderma congenitale: Rothmund-Thomson syndrome . Acta Dermatovener 39:392-420, 1959. 3. Carol WLL, Kooij R: Typus Maculatus der Bollosen Hereditären Dystrophie . Acta Dermatovener 18:265-283, 1937. 4. Curth HO, Warburton D: The genetics of incontinentia pigmenti . Arch Derm 92:229-235, 1965.Crossref 5. Franceschetti A, Jadassohn W: A propos de l'incontinentia pigmenti, delimitation de deux syndromes différents figurant sous le meme terme . Dermatologica 108:1-28, 1954.Crossref 6. Rollier MR: A propos de deux cas d'incontinentia pigmenti . Bull Soc France Derm Syph 67:122-125, 1960. 7. Kitamura K, Hirako T: Über zwei Japanische Fälle einer Eigenartigen Retikulären Pigmentierung: Zur Frage der Dermatose Pigmentaire Réticulée (Franceschetti-Jadassohn) . Dermatologica 110:97-107, 1955.Crossref 8. Vilanova X, Pinol Aguade J: Incontinentia pigmenti: Troubles sudoripares functionnels dysplasiques et pigmentaires chez les ascendants . Ann Derm Syph 86:247-258, 1959. 9. Jackli W: Ein Fall von Infantiler Poikilodermie (Atrophodermia Reticularis Com Incontinentia Pigmenti) Kombiniert mit Alopezie, Microdonite und Frühzeitiger Cataracta Complicata . Mschr Kinderheilk 78:73-81, 1939. 10. Hauser F, Pinkus H: Incontinentia pigmenti . Arch Derm 75:590, 1957. 11. Laguna C, Jaqueti G: Varedad reticular (tipo naegeli) de incontinencia pigmenti . Acta Derm 52:357-364, 1961. 12. Franceschetti A, Jadassohn W, Paillard R: Incontinentia pigmenti . Dermatologica 122:48-50, 1961.Crossref 13. Curth HO: Incontinentia pigmenti , in Genetik Pigmentarier Dermatosen , Ergänzungsband des Handbuches für Haut-und Geschlechtskrankheiten. Berlin, Springer-Verlag, 1965. 14. Degos R, Touraine R: Incontinentia pigmenti avec état poikilodermique . Bull Soc Franc Derm Syph 68:6-10, 1961. 15. Gahlen W: Dermatopathia pigmentosa reticularis hypohidrotica et atrophica . Derm Wschr 150:193-198, 1964. 16. Kindler T: Congenital poikiloderma with traumatic bulla formation and progressive cutaneous atrophy . Brit J Derm 66:104-111, 1954.Crossref 17. Weary PE, Hsu YT, Richardson DR, et al: Hereditary sclerosing poikiloderma: Report of two families with an unusual and distinctive genodermatosis . Arch Derm 100:413-422, 1969.Crossref http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Archives of Dermatology American Medical Association

Hereditary Acrokeratotic Poikiloderma

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Publisher
American Medical Association
Copyright
Copyright © 1971 American Medical Association. All Rights Reserved.
ISSN
0003-987X
eISSN
1538-3652
DOI
10.1001/archderm.1971.04000160059010
Publisher site
See Article on Publisher Site

Abstract

Abstract A dominantly inherited disorder has affected ten members of a family group. At present we recognize the following categories of clinical involvement: (1) vesicopustule formation which remains confined to the hands and feet (this process commences at from 1 to 3 months of age and resolves in late childhood); (2) widespread eczematous dermatitis somewhat resembling atopic eczema which starts between the ages of 3 and 6 months and completely resolves by 5 years of age; (3) the gradual appearance of a diffuse poikiloderma with striate and reticulate atrophy which spares only the face, scalp, and ears (the poikiloderma persists into adult life); and (4) the development of keratotic papules on the hands, feet, elbows, and knees, which first appear at varying times prior to 5 years of age and persist indefinitely. References 1. Costa OG: Acrokeratoelastoidosis . Derm Latin Amer 1:189-193, 1966. 2. Rook A, David R, Stevanovic D: Poikiloderma congenitale: Rothmund-Thomson syndrome . Acta Dermatovener 39:392-420, 1959. 3. Carol WLL, Kooij R: Typus Maculatus der Bollosen Hereditären Dystrophie . Acta Dermatovener 18:265-283, 1937. 4. Curth HO, Warburton D: The genetics of incontinentia pigmenti . Arch Derm 92:229-235, 1965.Crossref 5. Franceschetti A, Jadassohn W: A propos de l'incontinentia pigmenti, delimitation de deux syndromes différents figurant sous le meme terme . Dermatologica 108:1-28, 1954.Crossref 6. Rollier MR: A propos de deux cas d'incontinentia pigmenti . Bull Soc France Derm Syph 67:122-125, 1960. 7. Kitamura K, Hirako T: Über zwei Japanische Fälle einer Eigenartigen Retikulären Pigmentierung: Zur Frage der Dermatose Pigmentaire Réticulée (Franceschetti-Jadassohn) . Dermatologica 110:97-107, 1955.Crossref 8. Vilanova X, Pinol Aguade J: Incontinentia pigmenti: Troubles sudoripares functionnels dysplasiques et pigmentaires chez les ascendants . Ann Derm Syph 86:247-258, 1959. 9. Jackli W: Ein Fall von Infantiler Poikilodermie (Atrophodermia Reticularis Com Incontinentia Pigmenti) Kombiniert mit Alopezie, Microdonite und Frühzeitiger Cataracta Complicata . Mschr Kinderheilk 78:73-81, 1939. 10. Hauser F, Pinkus H: Incontinentia pigmenti . Arch Derm 75:590, 1957. 11. Laguna C, Jaqueti G: Varedad reticular (tipo naegeli) de incontinencia pigmenti . Acta Derm 52:357-364, 1961. 12. Franceschetti A, Jadassohn W, Paillard R: Incontinentia pigmenti . Dermatologica 122:48-50, 1961.Crossref 13. Curth HO: Incontinentia pigmenti , in Genetik Pigmentarier Dermatosen , Ergänzungsband des Handbuches für Haut-und Geschlechtskrankheiten. Berlin, Springer-Verlag, 1965. 14. Degos R, Touraine R: Incontinentia pigmenti avec état poikilodermique . Bull Soc Franc Derm Syph 68:6-10, 1961. 15. Gahlen W: Dermatopathia pigmentosa reticularis hypohidrotica et atrophica . Derm Wschr 150:193-198, 1964. 16. Kindler T: Congenital poikiloderma with traumatic bulla formation and progressive cutaneous atrophy . Brit J Derm 66:104-111, 1954.Crossref 17. Weary PE, Hsu YT, Richardson DR, et al: Hereditary sclerosing poikiloderma: Report of two families with an unusual and distinctive genodermatosis . Arch Derm 100:413-422, 1969.Crossref

Journal

Archives of DermatologyAmerican Medical Association

Published: Apr 1, 1971

References