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Page 1
Adermatoglyphia.
Alruwaili J, Hai A. Alruwaili J, et al. Natl Med J India. 2019 Jul-Aug;32(4):253. doi: 10.4103/0970-258X.291296. Natl Med J India. 2019. PMID: 32769257 Free article. No abstract available.
Adermatoglyphia in the Era of Biometrics.
De A, Dhar S, Sarda A, Dhar S. De A, et al. Indian J Dermatol. 2022 Jul-Aug;67(4):465-467. doi: 10.4103/ijd.ijd_54_21. Indian J Dermatol. 2022. PMID: 36578701 Free PMC article. No abstract available.
Adermatoglyphia: Barriers to Biometric Identification and the Need for a Standardized Alternative.
Sarfraz N. Sarfraz N. Cureus. 2019 Feb 8;11(2):e4040. doi: 10.7759/cureus.4040. Cureus. 2019. PMID: 31011502 Free PMC article. Review.
Dermatoglyphics form a vital portion of mass data collection, biometric scrutiny, and verification. Adermatoglyphia, or simply, loss of fingerprints attributed to a medical cause, represents a taxing situation for such biometric scrutiny systems requiring a fingerprint sca …
Dermatoglyphics form a vital portion of mass data collection, biometric scrutiny, and verification. Adermatoglyphia, or simply, loss …
Huriez syndrome: Additional pathogenic variants supporting allelism to SMARCAD syndrome.
Loh AYT, Špoljar S, Neo GYW, Escande-Beillard N, Leushacke M, Luijten MNH, Venkatesh B, Bonnard C, van Steensel MAM, Hamm H, Carmichael A, Rajan N, Carney TJ, Reversade B. Loh AYT, et al. Am J Med Genet A. 2022 Jun;188(6):1752-1760. doi: 10.1002/ajmg.a.62703. Epub 2022 Feb 25. Am J Med Genet A. 2022. PMID: 35212137
On the basis of phenotypic and genotypic convergence with Adermatoglyphia (OMIM136000) and Basan syndrome (OMIM129200), our results lend credence to the notion that these three Mendelian disorders are allelic. We propose adding Huriez syndrome to the previously suggested S …
On the basis of phenotypic and genotypic convergence with Adermatoglyphia (OMIM136000) and Basan syndrome (OMIM129200), our results l …
Capecitabine induced fingerprint loss: Case report and review of the literature.
Deneken-Hernandez Z, Cherem-Kibrit M, Gutiérrez-Andrade L, Rodríguez-Gutiérrez G, Colmenero-Mercado JO. Deneken-Hernandez Z, et al. J Oncol Pharm Pract. 2022 Mar;28(2):495-499. doi: 10.1177/10781552211045009. Epub 2021 Oct 5. J Oncol Pharm Pract. 2022. PMID: 34609922 Review.
INTRODUCTION: Adermatoglyphia is defined as the medical condition clinically diagnosed to those who have a congenital or acquired loss of the epidermal ridges on the fingertips, commonly known as fingerprints. ...In 2018, after two years on the fluoropyrimidine (capecitabi …
INTRODUCTION: Adermatoglyphia is defined as the medical condition clinically diagnosed to those who have a congenital or acquired los …
Capecitabine and adermatoglyphia: trouble in border!
Mazza C, Slimano F, Visseaux L, Ordan MA, Botsen D, Grange F, Bouche O. Mazza C, et al. J Eur Acad Dermatol Venereol. 2017 Jun;31(6):e283-e284. doi: 10.1111/jdv.14045. Epub 2016 Nov 28. J Eur Acad Dermatol Venereol. 2017. PMID: 27859657 No abstract available.
Individuals lacking ridge detail: A case study in adermatoglyphia.
Cook HI, Harrison K, James H. Cook HI, et al. J Forensic Sci. 2021 Jan;66(1):202-208. doi: 10.1111/1556-4029.14597. Epub 2020 Nov 2. J Forensic Sci. 2021. PMID: 33136290
Adermatoglyphia is a very rare autosomal-dominant condition that is genetically inherited and causes an individual to be born without conventional ridge detail on either their palmar or plantar surfaces (the fingers and palms of the hands and the toes and the soles of the …
Adermatoglyphia is a very rare autosomal-dominant condition that is genetically inherited and causes an individual to be born without …
Is adermatoglyphia an additional feature of Kindler Syndrome?
Almeida HL Jr, Goetze FM, Fong K, Lai-Cheong J, McGrath J. Almeida HL Jr, et al. An Bras Dermatol. 2015 Jul-Aug;90(4):592-3. doi: 10.1590/abd1806-4841.20153501. An Bras Dermatol. 2015. PMID: 26375235 Free PMC article.
We describe a rarely reported feature of two cases, one sporadic and one familial; both patients noticed acquired adermatoglyphia. The loss of dermatoglyphics could be an additional feature of this syndrome....
We describe a rarely reported feature of two cases, one sporadic and one familial; both patients noticed acquired adermatoglyphia. Th …
Ectodermal dysplasia with congenital adermatoglyphia (Basan syndrome): Report of two cases presenting with extensive congenital milia.
Nieto-Benito LM, Molina-López I, Feito-Rodríguez M, Martínez-González V, Suárez-Fernández R, Campos-Dominguez M. Nieto-Benito LM, et al. Pediatr Dermatol. 2021 Mar;38(2):530-532. doi: 10.1111/pde.14512. Epub 2021 Jan 24. Pediatr Dermatol. 2021. PMID: 33486784
Basan syndrome is a rare autosomal dominant genodermatosis, characterized by rapidly healing congenital acral bullae, congenital milia and adermatoglyphia (lack of finger and toeprints). This type of ectodermal dysplasia has been infrequently reported in the literature. .. …
Basan syndrome is a rare autosomal dominant genodermatosis, characterized by rapidly healing congenital acral bullae, congenital milia and …
A case of dermatopathia pigmentosa reticularis.
Bu TS, Kim YK, Whang KU. Bu TS, et al. J Dermatol. 1997 Apr;24(4):266-9. doi: 10.1111/j.1346-8138.1997.tb02787.x. J Dermatol. 1997. PMID: 9164071
Many other dermatologic findings have been associated with this triad, including adermatoglyphia, hypohidrosis or hyperhidrosis, palmoplantar hyperkeratosis, and nonscarring blisters on the dorsa of the hands and feet. ...We present a Korean patient with the typical featur …
Many other dermatologic findings have been associated with this triad, including adermatoglyphia, hypohidrosis or hyperhidrosis, palm …
32 results