A double whammy! Rare occurrence of psoriasis vulgaris in a case of X-linked recessive ichthyosis

被引：0

作者：

Jain, Akshay Kumar ^{[1
]}

Saini, Shivani ^{[3
]}

Agrawal, Nidhi ^{[2
]}

Agarwal, Shail ^{[4
]}

机构：

[1] Govt Med Coll, Dept Skin & VD, Kota, India

[2] Govt Med Coll, Dept Pathol, Kota, India

[3] Dr SN Med Coll, Dept Skin & VD, Jodhpur, Rajasthan, India

[4] Jhalawar Med Coll, Dept Skin & VD, Jhalawar, Rajasthan, India

来源：

INDIAN JOURNAL OF PAEDIATRIC DERMATOLOGY | 2021年 / 22卷 / 02期

关键词：

Epigenetics; genetic; psoriasis vulgaris; X-linked recessive ichthyosis; CHOLESTEROL-SULFATE;

D O I：

10.4103/ijpd.ijpd_167_20

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Ichthyosis and psoriasis both are inherently considered as disorders of abnormal keratinization. X-linked recessive ichthyosis (XLRI) is a genetic disorder, while psoriasis is sporadic in most cases. The underlying pathophysiology for their occurrence in the same patient is not well understood but may be attributed to genetic modifications or epigenetics. We hereby report a case of a 14-year-old male child with psoriasis vulgaris in the setting of XLRI. To our best knowledge, it has not been reported in the English literature to date.

引用

页码：165 / 167

页数：3

共 18 条

[1] Genetic Study of X-Linked Recessive Ichthyosis in Eastern Ukraine
O. M. Fedota
L. V. Roshcheniuk
I. O. Sadovnychenko
J. V. Gontar
I. M. Merenkova
V. M. Vorontsov
P. P. Ryzhko
Cytology and Genetics, 2021, 55 : 47 - 52
[2] Genetic Study of X-Linked Recessive Ichthyosis in Eastern Ukraine
Fedota, O. M.
Roshcheniuk, L. V.
Sadovnychenko, I. O.
Gontar, J. V.
Merenkova, I. M.
Vorontsov, V. M.
Ryzhko, P. P.
CYTOLOGY AND GENETICS, 2021, 55 (01) : 47 - 52
[3] Male-pattern baldness in men with X-linked recessive ichthyosis
Trüeb, RM
Meyer, JC
DERMATOLOGY, 2000, 200 (03) : 247 - 249
[4] Revisiting X-linked congenital ichthyosis
Zhou, Baishun
Liang, Cancan
Li, Peiyao
Xiao, Heng
INTERNATIONAL JOURNAL OF DERMATOLOGY, 2025, 64 (01) : 51 - 61
[5] Male-pattern baldness is common in men with X-linked recessive ichthyosis
Axt-Gadermann, M
Schlichting, M
Küster, W
DERMATOLOGY, 2003, 207 (03) : 308 - 309
[6] Novel point mutation in the STS gene in a patient with X-linked recessive ichthyosis
Winge, Marten C. G.
Hoppe, Torborg
Lieden, Agne
Nordenskjold, Magnus
Vahlquist, Anders
Wahlgren, Carl-Fredrik
Torma, Hans
Bradley, Maria
Berne, Berit
JOURNAL OF DERMATOLOGICAL SCIENCE, 2011, 63 (01) : 62 - 64
[7] TINEA-CORPORIS DUE TO TRICHOPHYTON-VERRUCOSUM IN RECESSIVE, X-LINKED ICHTHYOSIS
IBSEN, HHW
BRANDRUP, F
MYCOSES, 1993, 36 (9-10) : 319 - 320
[8] OCULAR FINDINGS IN X-LINKED ICHTHYOSIS - A SURVEY ON 38 CASES
COSTAGLIOLA, C
FABBROCINI, G
ILLIANO, GMP
SCIBELLI, G
DELFINO, M
OPHTHALMOLOGICA, 1991, 202 (03) : 152 - 155
[9] X-linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestations
Zhang, Min
Huang, Hailong
Lin, Na
He, Shuqiong
An, Gang
Wang, Yan
Chen, Meihuan
Chen, Lingji
Lin, Yuan
Xu, Liangpu
JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2020, 34 (05)
[10] CO-OCCURRENCE OF PRIMARY MICROCEPHALY CAUSED BY A NOVEL HOMOZYGOUS ASPM MUTATION ALONG WITH X-LINKED ICHTHYOSIS IN THE SAME PATIENT
Abdel-Hamid, M. S.
Ismail, M. F.
Darwish, H. A.
Effat, L. K.
Zaki, M. S.
Abdel-Salam, G. M. H.
GENETIC COUNSELING, 2016, 27 (01): : 25 - 33

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