Collodion baby: Ultrastructure and distribution of cornified cell envelope proteins and keratins

Dermatology

Volumn 195, Issue 2, 1997, Pages 164-168

  Akiyama, M ^a   Shimizu, H ^b   Yoneda, K ^c   Nishikawa, T ^b  

^a KITASATO INSTITUTE HOSPITAL   (Japan)

^b KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c KYOTO UNIVERSITY FACULTY OF MEDICINE   (Japan)

Author keywords

Collodion baby; Cornified cell envelope; Electron microscopy; Keratin; Lamellar ichthyosis

Indexed keywords

FILAGGRIN; INVOLUCRIN; KERATIN; LIPID; PROFILAGGRIN;

ARTICLE; CASE REPORT; CLINICAL FEATURE; ELECTRON MICROSCOPY; GRANULAR CELL; HUMAN; IMMUNOHISTOCHEMISTRY; KERATINOCYTE; LAMELLAR ICHTHYOSIS; MALE; PRIORITY JOURNAL;

EID: 0030751058     PISSN: 10188665     EISSN: 14219832     Source Type: Journal    
DOI: 10.1159/000245724     Document Type: Article

References (25)

1. Bloom D. Goodfried MS: Lamellar ichthyosis of the newborn. Arch Dermatol 1962:86: 336-342.
2. Williams ML. Elias PM: Genetically transmitted. generalized disorders of cornification: The ichthyoses. Dermatol Clin 1987;5:155-178.
3. Larrcgue M. Gharbi R, Daniel J. Le Marec Y. Civatte J: Le bebe collodion: Evolution a propos de 29 cas. Ann Dermatol Syphiligr 1976;103:31-56.
4. Frenk E, Mevorah B: The keratinization disorder in collodion babies evolving into lamellar ichthyosis: Its possible relevance for determining the primary defect in lamellar ichthyosis. J Cutan Pathol 1977:4:329-337.
5. Huber M. Rettler I, Bemasconi K. Frenk E. Lavrijsen SPM. Ponec M. Bon A. Lauten schlager S, Schorderet DF. Hohl D: Mutations of keratinocyte transglutaminase in lamellar ichthyosis. Science 1995;267:525-528.
6. Russell LJ, DiGiovanna JJ. Rogers GR. Stei-nert PM. Hashem N. Compton JG. Bale SJ: Mutations in the gene for transglutaminase I in autosomal recessive lamellar ichthyosis. Nat Genet 1995;9:279-283.
7. Hsu SM. Raine L. Fanger H: Use of avidin-biotin-peroxidase complex (ABC) in immu-noperoxidase technique: A comparison between ABC and unlabeled antibody (PAP) procedures. J Histochem Cytochcm 198l;29: 577-580.
8. Kim S-Y. Chung S-I. Yoneda K. Stcinert PM: Expression of transglutaminase I in human epidermis. J Invest Dermatol 1995:104:211-217.
9. Mehrel T. Hohl D. Rothnagel JA, Longley MA. Bundman D, Cheng C. Iichti U. Bisher ME, Steven AC. Steinert PM, Yuspa SH. Roop DR: Identification of a major keratinocyte cell envelope protein, loricrin. Cell 1990:61: 1103-1112.
10. Anton-Lamprecht I: The skin; in Papadimi-triou JM. Henderson DW, Spagnolo DV (cds): Diagnostic Ultrastructure of Noil-Neoplastic Diseases. Edinburgh. Churchill Livingstone. 1992. pp 459-550.
11. Haftek M. Cambazard F. Dhouailly D. Reano A. Simon M. Lachaux A. Serre G, Claudy A. Schmitt D: A longitudinal study of a harlequin infant presenting clinically as non-bullous congenital ichthyosiform erythroderma. Br J Dermatol 1996;135:448-453.
12. Arnold M-L, Anton-Lamprecht I. Melz-Roth-fuss B. Hartsehuh W: Ichthyosis congenita type III: Clinical and ultrastructural characteristics and distinction within the heterogeneous ichthyosis congenita group. Arch Dermatol Res 1988;280:268-278.
13. Nicmi K-M. Kanerva L: Ichthyosis with laminated membrane structures. Am J Dermato-pathol 1989;11:149-156.
14. Huber M. Rettler I, Bemasconi K, Wyss M. Hohl D: Lamellar ichthyosis is genetically heterogeneous - Cases with normal keratinocyte transglutaminase. J Invest Dermatol 1995:105: 653-654.
15. Hohl D. Huber M, Frenk E: Analysis of the cornified cell envelope in lamellar ichthyosis. Arch Dermatol 1993;129:618-624.
16. Dale BA. Holbrook KA. Fleckman P. Kimball JR, Brumbaugh S. Sybert VP: Heterogeneity in harlequin ichthyosis, an inborn error of epidermal keratinization: Variable morphology and structural protein expression and a defect in lamellar granules. J Invest Dermatol 1990:94: 6-18.
17. Milner ME. O’Guin WM. Holbrook KA. Dale BA: Abnormal lamellar granules in harlequin ichthyosis. J Invest Dermatol 1992;99: 824-829.
18. Hashimoto K. Khan S: Harlequin fetus with abnormal lamellar granules and giant mitochondria. J Cutan Pathol 1992:19:247-252.
19. Hashimoto K. De Dobbeleer G. Kanzaki T: Electron microscopic studies of harlequin fetuses. Pediatr Dermatol 1993:10:214-223.
20. Akiyama M. Kim D-K. Main DM. Otto CE. Holbrook KA: Characteristic morphologic abnormality of harlequin ichthyosis detected in amniotic fluid cells. J Invest Dermatol 1994: 102:210-213.
21. Akiyama M. Yoneda K. Kim S-Y. Koyama H. Shimizu H: Cornified cell envelope proteins and keratins are normally distributed in harlequin ichthyosis. J Cutan Pathol 1996:23: 571-575.
22. Akiyama M. Kim S-Y. Yoneda K. Shimizu H: Expression of transglutaminase I (transglutaminase K) in harlequin ichthyosis. Arch Dermatol Res 1997:289:116-119.
23. Dale BA. Kam E: Harlequin ichthyosis: Variability in expression and hypothesis for disease mechanism. Arch Dermatol 1993:129: 1471-1477.
24. Niemi K-M, Kanerva L. Kuokkamen K: Recessive ichthyosis congenita type 11. Arch Dermatol Res 1991:283:211-218.
25. Ghadially R. Williams ML. Hou SYE. Elias PM: Membrane structural abnormalities in the stratum corneum of the autosomal recessive ichthyoses. J Invest Dermatol 1992:99: 755-763.