Gong Z - Search Results

1

Three new founder mutations in Chinese patients with Nagashima-type palmoplantar keratoderma.

Liu J, Chen Z, Hu L, Song Z, Mo R, Tsang LS, Liu Y, Huang X, Gong Z, Xiang R, Lin Z, Yang Y. Liu J, et al. Among authors: gong z. Br J Dermatol. 2022 Dec;187(6):1043-1045. doi: 10.1111/bjd.21835. Epub 2022 Sep 7. Br J Dermatol. 2022. PMID: 35976164 No abstract available.

2

Investigation of Nagashima-type palmoplantar keratoderma in China: A cross-sectional study of 234 patients.

Liu J, Chen Z, Hu L, Song Z, Mo R, Tsang LS, Liu Y, Huang X, Gong Z, Lin Z, Yang Y. Liu J, et al. Among authors: gong z. J Dermatol. 2023 Mar;50(3):375-382. doi: 10.1111/1346-8138.16621. Epub 2022 Nov 1. J Dermatol. 2023. PMID: 36317385

3

Variants in KLK11, affecting signal peptide cleavage of kallikrein-related peptidase 11, cause an autosomal-dominant cornification disorder.

Gong Z, Dai S, Jiang X, Lee M, Zhu X, Wang H, Lin Z. Gong Z, et al. Br J Dermatol. 2023 Jan 23;188(1):100-111. doi: 10.1093/bjd/ljac029. Br J Dermatol. 2023. PMID: 36689511

4

PLACK syndrome caused by novel pathogenic variants in CAST: a case report and literature review.

Hu B, Gong Z, Peng S, Wang H, Chen L, Lin Z. Hu B, et al. Among authors: gong z. Clin Exp Dermatol. 2023 Aug 25;48(9):1052-1055. doi: 10.1093/ced/llad167. Clin Exp Dermatol. 2023. PMID: 37140444 Review. No abstract available.

5

Skin biopsy findings in megaconial congenital muscular dystrophy with psoriasiform lesions due to variants in CHKB.

Gong Z, Chen K, Xu Z, Yang Z, Wang H, Lin Z. Gong Z, et al. J Eur Acad Dermatol Venereol. 2024 Apr;38(4):e323-e325. doi: 10.1111/jdv.19598. Epub 2023 Nov 10. J Eur Acad Dermatol Venereol. 2024. PMID: 37907281 No abstract available.

6

Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformation.

Jiang X, Yang C, Wang Z, Liang L, Gong Z, Huang S, Xu Z, Zhang B, Pei X, Cai L, Wang H, Lin Z. Jiang X, et al. Among authors: gong z. Br J Dermatol. 2024 Jun 20;191(1):107-116. doi: 10.1093/bjd/ljae108. Br J Dermatol. 2024. PMID: 38489583

7

Treatment of autosomal recessive congenital ichthyosis caused by a NIPAL4 variant with upadacitinib.

Gong Z, Wang Y, Jiang X, Wang H, Lin Z. Gong Z, et al. J Eur Acad Dermatol Venereol. 2025 Jan;39(1):e91-e93. doi: 10.1111/jdv.20130. Epub 2024 May 29. J Eur Acad Dermatol Venereol. 2025. PMID: 38808853 No abstract available.

8

Dermatopathological features and successful treatment with topical antioxidant for ichthyosiform lesions in Mitchell syndrome caused by an ACOX1 variant.

Gong Z, Yang S, Ling S, Wang H, Xu X, Lin Z. Gong Z, et al. J Dermatol. 2024 Jun 24. doi: 10.1111/1346-8138.17346. Online ahead of print. J Dermatol. 2024. PMID: 38923010

9

A gain-of-function variant in SREBF1 causes generalized skin hyperpigmentation with congenital cataracts.

Wang H, Wu Y, Bassetti JA, Wang Z, Oza VS, Rangu SA, McGivern B, Peng S, Liang L, Huang S, Gong Z, Xu Z, Lin Z. Wang H, et al. Among authors: gong z. Br J Dermatol. 2024 Oct 17;191(5):805-815. doi: 10.1093/bjd/ljae291. Br J Dermatol. 2024. PMID: 39005171

10

Unilateral focal palmoplantar keratoderma associated with a postzygotic variant in PIK3CA and activation of the PI3K/AKT/mTOR pathway.

Gong Z, Peng S, Wang H, Jiang X, Ke X, Lin Z. Gong Z, et al. Eur J Dermatol. 2024 Jun 1;34(3):287-293. doi: 10.1684/ejd.2024.4704. Eur J Dermatol. 2024. PMID: 39015962

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