Literature DB >> 20619487

The immigration delay disease: adermatoglyphia-inherited absence of epidermal ridges.

Bettina Burger1, Dana Fuchs, Eli Sprecher, Peter Itin.   

Abstract

In the digital age, personal identification by fingerprints (epidermal ridges) has become more frequent and is often required for biometric passports. The more fingerprints are analyzed, the more variants in their formation are documented. Individuals completely missing fingerprints as an isolated finding are extremely rare. Only 4 kindreds have been described to date, with additional clinical features in most cases. We describe a female patient with missing epidermal ridges on the fingers, palms, toes, and soles as an isolated feature. Absent fingerprints, or adermatoglyphia, were inherited over 4 generations of her family in an autosomal dominant fashion. We present the clinical features of the index patient, and compare the case with previous reports in the literature. Because of problems in personal identification, this embryologic malformation caused the patient significant difficulties when traveling to other countries, which is why we name it the immigration delay disease.
Copyright © 2009 American Academy of Dermatology, Inc. Published by Mosby, Inc. All rights reserved.

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Year:  2010        PMID: 20619487     DOI: 10.1016/j.jaad.2009.11.013

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  7 in total

1.  A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia.

Authors:  Janna Nousbeck; Bettina Burger; Dana Fuchs-Telem; Mor Pavlovsky; Shlomit Fenig; Ofer Sarig; Peter Itin; Eli Sprecher
Journal:  Am J Hum Genet       Date:  2011-08-04       Impact factor: 11.025

2.  Association between Mutation in SMARCAD1 and Basan Syndrome with Cutaneous Squamous Cell Carcinoma.

Authors:  Ying Xiong; Ting Chen; Jia Yu; He Zhou; Baozhen Lu; Lijie Chen; Liwei Sun; Can Wang; Sujun Li; Bo Wu
Journal:  Dis Markers       Date:  2022-05-10       Impact factor: 3.464

3.  Genome-wide linkage analysis and whole-genome sequencing identify a recurrent SMARCAD1 variant in a unique Chinese family with Basan syndrome.

Authors:  Ming Li; Jianbo Wang; Zhenlu Li; Jia Zhang; Cheng Ni; Ruhong Cheng; Zhirong Yao
Journal:  Eur J Hum Genet       Date:  2016-03-02       Impact factor: 4.246

4.  Acropigmentation of Kitamura with immigration delay disease: A rare entity.

Authors:  Sumir Kumar; Bharat Bhushan Mahajan; Nidhi Kamra; Pritish A Bhoyar
Journal:  Indian Dermatol Online J       Date:  2015 May-Jun

5.  A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association.

Authors:  Sumir Kumar; Pritish Bhoyar; Bharat Bhushan Mahajan
Journal:  Indian Dermatol Online J       Date:  2015 Mar-Apr

6.  Two SMARCAD1 Variants Causing Basan Syndrome in a Canadian and a Dutch Family.

Authors:  Youssef Elhaji; Tessa M A van Henten; Claudia A L Ruivenkamp; Mathew Nightingale; Gijs We Santen; Lydia E Vos; Peter R Hull
Journal:  JID Innov       Date:  2021-05-06

7.  Capecitabine-Associated Loss of Fingerprints: A Case Report of a 62-Year-Old Man With Colorectal Cancer Suffering From Capecitabine-Induced Adermatoglyphia.

Authors:  Tasneem Dawood; Muhammad Nauman Zahir; Muhammad Afzal; Yasmin Abdul Rashid
Journal:  Cureus       Date:  2021-06-08
  7 in total

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