Severe congenital generalized exfoliative erythroderma in newborns and infants: A possible sign of Netherton syndrome

Pediatric Dermatology

Volumn 13, Issue 3, 1996, Pages 183-199

  Hausser, Ingrid ^a,b   Anton Lamprecht, Ingrun ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b Inst Ultrastructure Res Skin   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ATOPY; CLINICAL ARTICLE; CLINICAL EXAMINATION; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; DISEASE COURSE; ELECTRON MICROSCOPY; FEMALE; HUMAN; INFANT; INFANT DISEASE; MALE; NEWBORN; NEWBORN DISEASE; PRIORITY JOURNAL; SYNDROME;

EID: 0029886303     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1525-1470.1996.tb01202.x     Document Type: Article

References (47)

1. Netherton EW. A unique case of trichorrhexis nodosa "bamboo hairs." Arch Dermatol 1958;78:483-487.
2. Altmann J. Stroud J. Netherton's syndrome and ichthyosis linearis circumflexa. Arch Dermatol 1969; 100:550-558.
3. Hersle K. Netherton's disease and ichthyosis linearis circumflexa. Report of a case and review of the literature. Acta Derm Venereol 1972;52:298-302.
4. Frenk E, Mevorah B. Ichthyosis linearis circumflexa Comèl with trichorrhexis invaginata (Netherton's syndrome). An ultrastructural study of the skin changes. Arch Dermatol Forsch 1972;245:42-49.
5. Zina AM, Bundino S. Ichthyosis linearis circumflexa Comèl und Netherton-Syndrom. Eine ultrastruktureile Studie. Dermatologica 1979;158:404-412.
6. Hausser I, Anton-Lamprecht I, Hartschuh W, Petzoldt D. Netherton's syndrome: Ultrastructure of the active lesion under retinoid therapy. Arch Dermatol Res 1989;281:165-172.
7. Traupe H. The ichthyoses. A guide to clinical diagnosis, genetic counseling, and therapy. New York: Springer-Verlag, 1990.
8. Anton-Lamprecht I, Arnold ML. The skin of the newborn under normal and pathological conditions. In: Caputo R, Gelmetti C, eds. Proceedings of the 5th International Congress of Pediatric Dermatology. Milan: Cilag Pharma, 1989.
9. Traupe H. Hamm H. Recent advances in genetic hair disease. H + G Z Hautkrankh 1990;65:1085-1091
10. Plantin P, Delaire P, Guillet MH, Labouche F, Guillet G. Syndrome de Netherton. Aspects actuels. A propos de neuf cas. Ann Dermatol Venereol 1991; 118:525-530.
11. Giroux JD, Sizun J, Gardach C, Awad H, Guillos B, Alix D. Déshydratation hypernatrémique sévère révélant un syndrome de Netherton en période néonatale. Arch Fr Pediatr 1993;50:585-588.
12. Jones SK, Thomason LM, Surbrugg SK, Weston WL. Neonatal hypernatraemia in two siblings with Netherton's syndrome. Br J Dermatol 1986;114:741-743.
13. Anton-Lamprecht I. Erkrankungen und Entwicklungsstörungen des Haarschaftes. Swiss Med 1985; 7(5b):41-50.
14. Peracchia C, Mittler BS. Fixation by means of glutaraldehyde-hydrogen peroxide reaction products. J Cell Biol 1972:53:234-238.
15. Anton-Lamprecht I. The skin. In: Papadimitriou JM, Henderson DW, Spagnolo DV , eds. Diagnostic ultrastructure of non-neoplastic diseases. Edinburgh: Churchill Livingstone, 1992:459-550.
16. Greene SL, Muller SA. Netherton's syndrome. Report of a case and review of the literature. J Am Acad Dermatol 1985;13:329-337.
17. Larrègue M, Bressieux JM. Bonafé JL, et al. Trichorrhexie invaginata et érythrodermie acrofigurée: héterogenéité du syndrome dit de "Netherton." Ann Dermatol Venereol 1989;116:685.
18. Heule F, Vuzevsky KD, Tio TT. Netherton's syndrome. Br J Dermatol 1990;123:269-270.
19. Judge MR, Morgan G, Harper JI. A clinical and immunological study of Netherton's syndrome. Br J Dermatol 1994;131:615-621.
20. Seraly MP, Sheehan M. Collins M, Mostow E. Netherton syndrome revisited. Pediatr Dermatol 1994;16: 61-64.
21. Larrègue M, Ottavy N, Bressieux JM, Lorette J. Collodion baby: 32 new cases. Ann Dermatol Venereol 1986;113:773-785.
22. Petzoldt D, Anton-Lamprecht I. Ichthyosis congenita - Ein Sammeltopf verschiedener Verhornungsstörungen? Hautarzt 1983;34(suppl VI):22-24.
23. Elias PM, Fritsch P, Epstein EH. Staphylococcal scalded skin syndrome. Arch Dermatol 1977;113: 207-219.
24. Hagberg BA, Blennow G, Kristiansson B, Stibler H. Carbohydrate-deficient glycoprotein syndromes: Peculiar group of new disorders. Pediatr Neurol 1993;9: 255-262.
25. Pupo RA, Tyring SK, Raimer SS, Wirt DP, Brooks EG, Goldblum RM. Omenn's syndrome and related combined immunodeficiency syndromes: Diagnostic considerations in infants with persistent erythroderma and failure to thrive. J Am Acad Dermatol 1991;25:442-446.
26. Gaber G, Klöditz, Lichtenberger O, Fiedler H, Wozniak KD. Netherton-Syndrom. X. Congress of the Gesellschaft für Dermatologie der DDR, Dresden. 1990.
27. Krafchik BR. Netherton syndrome. Pediatr Dermatol 1987;9:157-160.
28. Kahn D, Altman J. Hutchinson E. Lamellar ichthyosis with episodic psoriasiform reaction pattern. Cutis 1986;3:162-164.
29. Koch H, Holtvogt J, Arnold ML, Anton-Lamprecht I. Tödlich verlaufendes Netherton-Syndrom unter dem Bild einer schweren Erythrodermie mit Hypernaträmie bei 2 Geschwistern. Monatsschr Kinderheilkd 1993;141:S64.
30. Fartasch M, Arnold ML, Bergman R. Characterization of barrier structures in different types of hereditary ichthyoses. J Invest Dermatol 1994; 103:260.
31. Fartasch M, Williams ML. Elias PM. Alterations in barrier formation and epidermal differentiation in Netherton's syndrome. Arch Dermatol 1994;286:221.
32. Pohl M, Zimmerhackl LB, Hausser I, et al. Akute bilaterale Nierenvenenthrombose als Komplikation des Netherton-Syndroms. Poster at 38. Tagung der Gesellschaft für Kinderheilkunde, Hannover, 9/1994.
33. Hintner H, Jaschke E, Fritsch P. Netherton-Syndrom: Abwehrschwäche, generalisierte Verrukose und Karzinogenese. Hautarzt 1990;31:428-432.
34. Moffatt MF, Hill MR, Cornélis F, et al. Genetic linkage of T-cell receptor lambda/delta complex to specific IgE responses. Lancet 1994;343:1597-1600.
35. Hartschuh W, Hausser I, Petzoldt D. Erfolgreiche Retinoidtherapie des Netherton-Syndroms. Hautarzt 1989;40:430-433.
36. Kopan R, Traska G, Fuchs E. Retinoids as important regulators of terminal differentiation: Examining keratin expression in individual epidermal cells at various stages of keratinization. J Cell Biol 1987;105:427-440.
37. Fritsch P. Austrian experience with etretinate. In: Cuncliffe WJ, Miller AJ. eds. Retinoid therapy. A review of clinical and laboratory research. Lancaster: MTP Press, 1984:45-54.
38. Traupe H, Happle R. Etretinate therapy in children with severe keratinization disorders. Eur J Pediatr 143:166-169.
39. Imakado S, Bickenbach JR, Bundman DS, et al. Targeting expression of a dominant-negative retinoic acid receptor mutant in the epidermis of transgenic mice results in loss of barrier function. Genes Dev 1995;9:317-329.
40. de Berker DAR, Paige DG, Ferguson DJP, Dawber RPR. Golf tee hairs in Netherton disease. Pediatr Dermatol 1995;12:7-11.
41. Price VH. Strukturanomalien des Haarschaftes. In: Orfanos CE, ed. Haar und Haarerkrankungen, 2nd ed. Stuttgart: Gustav Fischer Verlag, 1991:387-446.
42. Hashimoto K, Niizuma K. Hair abnormalities. In: Hashimoto K, Niizuma K. eds. Skin pathology by light and electron microscopy. Tokyo: Igaku-Shoin, 1983:229-247.
43. Nolting S, Ulbricht H. Nagelmykosen. In: Nolting S, ed. Ciclopriroxolamin: Wegweiser topischer Mykose-Therapie. Jena FRG: Universitäts verlag, 1993.
44. Kvedar JC, Baden HP. Nail changes in cutaneous disease. Semin Dermatol 1991;10:65-70.
45. Orfanos CE, Mahrle G, Salomon T. Netherton-Syndrom. Ichthyosiforme Hautveränderungen und Trichorrhexis invaginata. Nachweis eines veränderten Cortexkeratins im Haar. Hautarzt 1971;22: 397-409.
46. Hall JG. Prenatal diagnosis of inherited skin diseases. Birth Defects 1981;17:243-255.
47. Anton-Lamprecht I. Pränatale Diagnose von Genodermatosen. Hautarzt 1988;39(suppl VIII):16-20.