A Family with Palmar and Plantar Hyperkeratosis: A Quiz

A Family with Palmar and Plantar Hyperkeratosis: A Quiz

Abstract is missing (Quiz)

Bibliographic Details
Main Authors:	Hazem A. Juratli, Sabine Jägle, Rudolf Happle, Pinar Avci, Dario Didona, Judith Fischer
Format:	Article
Language:	English
Published:	Society for Publication of Acta Dermato-Venereologica 2020-02-01
Series:	Acta Dermato-Venereologica
Subjects:	hereditary palmoplantar keratodermas, unna-thost, vörner, keratin 1, keratinopathic ichthyosis, epidermolytic palmoplantar keratoderma
Online Access:	https://www.medicaljournals.se/acta/content/html/10.2340/00015555-3419

Similar Items

Hereditary palmoplantar keratoderma: A practical approach to the diagnosis
by: Tanvi Dev, et al.
Published: (2019-01-01)

Exome sequencing identifies a KRT9 pathogenic variant in a Chinese pedigree with epidermolytic palmoplantar keratoderma
by: Changxing Li, et al.
Published: (2019-07-01)

Severe hereditary punctate palmoplantar keratoderma (Brauer-Buschke-Fischer syndrome)
by: Dorota Jaśkiewicz-Nyckowska, et al.
Published: (2015-06-01)

Punctate Palmoplantar Keratoderma
by: Susana Cláudia Teixeira, et al.
Published: (2021-09-01)

Punctate Palmoplantar Keratoderma
by: Susana Cláudia Teixeira, et al.
Published: (2021-09-01)

Unilateral Linear Punctate Palmoplantar Keratoderma: A Case Report
by: Chanisa Kiatsurayanon, et al.
Published: (2017-03-01)

Ichthyosis vulgaris and pycnodysostosis: An unusual occurrence
by: Vinayak Y. Kshirsagar, et al.
Published: (2012-11-01)

Diagnosis and Management of Inherited Palmoplantar Keratodermas
by: Bjorn R. Thomas, et al.
Published: (2020-03-01)

Hiperceratose focal acral: relato de caso e discussão sobre as ceratodermias marginais Focal acral hyperkeratosis: case report and discussion on marginal keratodermas
by: Maurício Zanini
Published: (2006-10-01)

A Case Report of Ichthyosis Lamellar Syndrome
by: Gholamreza Eshghi, et al.
Published: (2014-06-01)

Richner-Hanhart Syndrome (Tyrosinemia Type II) A Case Report of Delay Diagnosis with Hyperkeratotic Lesions of Palmes and Soles
by: Zahra Alian
Published: (2014-12-01)

Hiperqueratose palmo-plantar epidermolítica (Vörner) relato de caso e revisão da literatura Epidermolytic palmoplantar keratoderma (Vörner type) case report and revision of literature
by: Alexandre Bortoli Machado, et al.
Published: (2002-10-01)

Palmo-plantar hyperkeratosis associated with HTLV-1 infection: a case report
by: Elías Quintero-Muñoz, et al.
Published: (2021-07-01)

Beneficial Impact of Apremilast on Palmoplantar Keratodermas
by: Kimiko Nakajima, et al.
Published: (2021-04-01)

A study on palmoplantar keratodermas in childhood in a district hospital
by: Neerja Puri
Published: (2017-01-01)

Small Cell Variant of T-Cell Prolymphocytic Leukemia with Acquired Palmoplantar Keratoderma and Cutaneous Infiltration
by: Buthaina Al-Musalhi, et al.
Published: (2016-01-01)

Anesthetic considerations of Palmoplantar Keratoderma (PPK), a case report.
by: Parisa Sezari, et al.
Published: (2020-03-01)

Erythrokeratoderma en cocardes – A rare phenotype
by: P Arunprasath, et al.
Published: (2020-01-01)

Papillon-Lefevre syndrome with pseudoainhum
by: P Ashwani, et al.
Published: (2010-01-01)

A novel mutation resulting in keratin 1–linked palmoplantar keratoderma with epidermolytic ichthyosis
by: Taylor Gray, DO, et al.
Published: (2020-10-01)

Pachyonychia Congenita type 1 – A peerless entity
by: Yugandar Inakanti, et al.
Published: (2015-07-01)

Punctate Palmoplantar Keratoderma: A Case Report of Type 1 (Buschke-Fischer-Brauer Disease)
by: Rahaf Bukhari, et al.
Published: (2019-10-01)

Você conhece esta síndrome? Do you know this syndrome?
by: Isabela Guimarães Ribeiro Baeta, et al.
Published: (2011-06-01)

A Small Indel Mutant Mouse Model of Epidermolytic Palmoplantar Keratoderma and Its Application to Mutant-specific shRNA Therapy
by: Ya-Su Lyu, et al.
Published: (2016-01-01)

Genetic Analysis of KRT9 Gene Revealed Previously Known Mutations and Genotype-Phenotype Correlations in Epidermolytic Palmoplantar Keratoderma
by: Yuwei Li, et al.
Published: (2019-01-01)

Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma
by: Heng Xiao, et al.
Published: (2018-04-01)

Deafness, palmoplantar hyperkeratosis, and knuckle pads with male-to-male transmission: Bart-Pumphrey syndrome
by: Gisele Viana de Oliveira, et al.
Published: (2003-01-01)

Mal de Meleda : a case successfully treated with acitretin
by: Kaoutar Achehboune, et al.
Published: (2020-04-01)

Palmoplantar hyperkeratotic projections
by: Wendi Bao, BS, et al.
Published: (2020-10-01)

Leukoencephalopathy and Keratoderma
by: J Gordon Millichap
Published: (1995-02-01)

Woolly hair with palmoplantar keratoderma without cardiac abnormality: A rare case report
by: Saritha Mohanan, et al.
Published: (2020-01-01)

Pachyonychia Congenita (K16) with Unusual Features and Good Response to Acitretin
by: Fahad Almutawa, et al.
Published: (2015-08-01)

Pachyonychia congenita: A rare genodermatosis
by: Puneet Agarwal, et al.
Published: (2013-01-01)

Papillon-Lefevre syndrome: A case report with review of literature
by: Rajeev Gadgil, et al.
Published: (2009-01-01)

Mal de Meleda: A Report of Two Cases In One Family
by: M.Kantor, et al.
Published: (2006-08-01)

Olmsted syndrome with lateral supraciliary madarosis and clubbing: A rare case report
by: Md Zeeshan, et al.
Published: (2018-01-01)

Mal de Meleda: relato de 2 casos de ocorrência familiar Mal de Meleda: a report of two cases of familial occurrence
by: Fernanda Ayres de Morais e Silva, et al.
Published: (2011-08-01)

Keratin 17 mutations in four families from India with pachyonychia congenita
by: Manoj Agarwala, et al.
Published: (2017-01-01)

Use of Removable Partial Denture in Child with Papillon-Lefevre Syndrome: Case Report
by: Tania Saskianti, et al.
Published: (2020-07-01)

A Case Report of Keratoderma and Bilateral Deafness
by: Gholamreza Eshghi, et al.
Published: (2014-03-01)

Cannot write session to /tmp/vufind_sessions/sess_29cqu1f5pm3a2390r2os318lkq