Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads ( <scp>PLACK</scp> ) Syndrome: An Updated Review of Cases and Identification of a Recurrent <scp> <i>CAST</i> </scp> Variant in Two Patients

Peeling skin, leukonychia, acral punctate keratoses, cheilitis, and knuckle pads (PLACK) syndrome (OMIM616295) is an exceptionally rare autosomal recessive genodermatosis caused by loss-of-function pathogenic variants in the CAST gene, encoding calpastatin. A total of 19 cases have been described in 12 articles, among families with unique de novo genetic variants of CAST. We describe two pediatric PLACK cases with a homozygous loss-of-function CAST variant (c.571G>T, p.Gly191Ter) which represents the only recurrent genetic variant of PLACK syndrome reported in the literature.

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Publication Details

Journal
Pediatric Dermatology
Published
2025-05-19
DOI
https://doi.org/10.1111/pde.15987
Citations
1
Primary Topic
Skin and Cellular Biology Research
Type
article
Field-Weighted Citation Impact
1.15
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article

Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads ( PLACK ) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two Patients

Janan Mohamad, Ofer Sarig, Michele Ramien, Dana Boctor et al.
1 citations
Pediatric Dermatology
Skin and Cellular Biology Research
1.15
article

Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads ( PLACK ) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two Patients

Janan Mohamad, Ofer Sarig, Michele Ramien, Dana Boctor, Richard M. Haber, Fiona Haxho, Eli Sprecher, Renée Perrier
article en
1 citations

Abstract

Peeling skin, leukonychia, acral punctate keratoses, cheilitis, and knuckle pads (PLACK) syndrome (OMIM616295) is an exceptionally rare autosomal recessive genodermatosis caused by loss-of-function pathogenic variants in the CAST gene, encoding calpastatin. A total of 19 cases have been described in 12 articles, among families with unique de novo genetic variants of CAST. We describe two pediatric PLACK cases with a homozygous loss-of-function CAST variant (c.571G>T, p.Gly191Ter) which represents the only recurrent genetic variant of PLACK syndrome reported in the literature.

Pediatric DermatologyVol. 42(6)
Tel Aviv University (IL), University of Calgary (CA), Tel Aviv Sourasky Medical Center (IL), Alberta Children's Hospital (CA)
Openalex Percentile: Top 24%
Skin and Cellular Biology Research
1.15
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Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads ( <scp>PLACK</scp> ) Syndrome: An Updated Review of Cases and Identification of a Recurrent <scp> <i>CAST</i> </scp> Variant in Two Patients — Janan Mohamad, Ofer Sarig, et al. · Pediatric Dermatology (2025) | TGRS Research Map | TGRS