72 -7 (45) 2022 — Jumanov Z.E., Abdullaev S.D. — CHARACTERISTICS OF CLIMATE CONDITIONS OF STRATUM CORNEUM OF SKIN IN CONGENITAL ICHTYOSIS DISEASE SKIN CHANGES IN CONGENITAL ICHTYOSIS DISEASE

CHARACTERISTICS OF CLIMATE CONDITIONS OF STRATUM CORNEUM OF SKIN IN CONGENITAL ICHTYOSIS DISEASE SKIN CHANGES IN CONGENITAL ICHTYOSIS DISEASE

Jumanov Z.E., Samarkand State Medical University

Abdullaev S.D. Samarkand State Medical University

Resume

This article examines the morphological changes in skin structures depending on climatic conditions in congenital ichthyosis and identifies morphometric parameters. Skin changes at different times of the year were compared and analyzed. Different aspects were identified during the analysis process.

Keywords: Ichthyosis; horn floor; thorny floor; suction floor; glossy floor.

First page

381

Last page

384

For citation: Jumanov Z.E., Abdullaev S.D. CHARACTERISTICS OF CLIMATE CONDITIONS OF STRATUM CORNEUM OF SKIN IN CONGENITAL ICHTYOSIS DISEASE SKIN CHANGES IN CONGENITAL ICHTYOSIS DISEASE //New Day in Medicine 7(45)2022 381-384 https://clck.ru/sNusD

LIST OF REFERENCES:

1. Dvoryankova Ye.V., Mel’nichenko O.O., Krasnikova V.N., Korsunskaya I.M. Ixtioz. Chto vajno znat’ spesialistu. RMJ. Medisinskoe obozrenie. 2019; 12:25–30.
2.   Kaplunov K.O. Sluchay vrojdennogo vul’garnogo ixtioza u rebenka na fone pervichnogo immunodefisita // Volgogradiskiy nauchno-medisinskiy jurnal 2/2017 -S.45-48.
3. Kondrat’eva Yu.S., Safonov N.E., Kleymush V.A. Shipilov A. A. Semeyniy sluchay ixtioza. // Vestnik dermatologii i venerologii. – 2017. – № 4. – S.73 – 79. eLIBRARY ID: 16824806
4. Koshkin S.V., Chermnix T.V. Yevseeva A.L., Ryabova V.V., Ryabov A.N. Lamellyarniy vrojdenniy ixtioz. // Vestnik dermatologii i venerologii. – 2016. – № 5. – S 44 – 50. eLIBRARY ID: 27314558
5. Orlovskaya I.V., Ryumina I.I., Perepelkina A.E. Vrojdenniy ixtioz. // Rossiyskiy vestnik perinatologii i pediatrii. – 2016 – T. 54, № 6. – S. 22-25. eLIBRARY ID: 13065979
6.      Ishida-Yamamoto A., Eady RA, Underwood RA, Dale BA, Holbrook KA (1994). Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis). Br J Dermatol 131:767-779.
7. Brown S.J.,Relton C.L., Liao H., Zhao Y., Sandilands A., McLean W.H. et al.Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children//Br J Dermatol. 2009; 161: 884-889
8. Bueno E.et al., Novel mutations in FATP4 gene in two families with ichthyosis prematurity syndrome. J. Eur. Acad. Dermatol. Venereol. 31, e11–e13 (2017).
9. Bygum, Anette Westermark, Per Brandrup, Flemming. (2008). Ichthyosis prematurity syndrome: A well-defined congenital ichthyosis subtype. Journal of the American Academy of Dermatology. 59. S71-4. 10.1016/j.jaad.2008.06.014.
10. Dreyfus I., Pauwels C., Bourrat E., Bursztejn A.C., Maruani A., Chiaverini C., et al. Burden of inherited ichthyosis: a French national survey. Acta Derm Venereol. 2015;95(3): 326–8.
11. Goleva E., Berdyshev E., Leung D.Y. Epithelial barrier repair and prevention of allergy. // J Clin Invest 2019;129:1463-74.
12. Hotz V. Johansson, Per Karimi, Arizo. (2018). Parenthood, Family Friendly Workplaces, and the Gender Gaps in Early Work Careers. SSRN Electronic Journal. 10.2139/ssrn.3236426.
13. Khnykin D., J. H. Miner, F. Jahnsen, Role of fatty acid transporters in epidermis: Implications for health and disease. Dermatoendocrinol. 3, 53–61 (2011).
14. Klar J. et al., Mutations in the fatty acid transport protein 4 gene cause the ichthyosis prematurity syndrome. Am. J. Hum. Genet. 85, 248–253 (2009).
15. Miyamoto M , Itoh N , Sawai M , Sassa T , Kihara A. (2020) Severe skin permeability barrier dysfunction in knockout mice deficient in a fatty acid ω-hydroxylase crucial to acylceramide production. // J Invest Dermatol, 140, 319-326
16. Ohno Y., Nara A., Nakamichi S., A. Kihara A/Molecular mechanism of the ichthyosis pathology of Chanarin–Dorfman syndrome: Stimulation of PNPLA1-catalyzed ω-O-acylceramide production by ABHD5 // Journal of Dermatological Science 92 (2018) 245–253 DOI:https://doi.org/10.1016/j.jdermsci.2018.11.005
17. Oji V., Hautier J. M., Ahvazi B.et al., “Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype,” Human Molecular Genetics, vol. 15, no. 21, pp. 3083–3097, 2006.
18. Oji V.et al., Revised nomenclature and classification of inherited ichthyoses: Results  of the First Ichthyosis Consensus Conference in Sorèze 2009. J. Am. Acad. Dermatol. 63, 607–641 (2010).
19. Vahlquist A, Fischer J, Törmä HInherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment // Am J Clin Dermatol. 2018 Feb;19(1):51-66. doi: 10.1007/s40257-017-0313-x.
20. Zeng Y.P. [et al.] A recurrent missense mutation of keratin 1 gene in a Chinese family with epidermolytic hyperkeratosis (severe palmoplantar hyperkeratosis, type 1) / Y.P. Zeng [et al.] // Int J Dermatol. – 2012. – Vol. 51, № 2. – P. 182-185.