Cargando…

Poikiloderma a varied presentation - Huriez syndrome

Huriez syndrome is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma (PPK) and hypoplastic nails. We report the case of a 25 year old male, with nonfamilial Huriez syndrome.

Detalles Bibliográficos
Autores principales:	Kharge, Priyadarshini, Fernendes, Carol, Jairath, Vijayeeta, Mohan, Madan, Chandra, Suresh
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2015
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314883/ https://www.ncbi.nlm.nih.gov/pubmed/25657913 http://dx.doi.org/10.4103/2229-5178.148929

Ejemplares similares

Huriez syndrome with superadded dermatophyte infection
por: Surana, Trupti, et al.
Publicado: (2016)

Hereditary Sclerosing Poikiloderma
por: Lee, Hyo Jin, et al.
Publicado: (2012)

A Case of Poikiloderma Vasculare Atrophicans
por: Choi, Myoung-Soon, et al.
Publicado: (2011)

Poikiloderma with neutropenia: An alternate presentation with dyspigmentation and novel USB1 mutation
por: Peterson, Malina Yamashita, et al.
Publicado: (2022)

Creeping Eruption on the Move: A Case Series from Northern India
por: Kaur, Sarabjit, et al.
Publicado: (2015)

Nonfamilial Multiple Trichoepithelioma: Few and Far Between
por: Sehrawat, Manu, et al.
Publicado: (2016)

Erythroderma and extensive poikiloderma – a rare initial presentation of dermatomyositis: a case report
por: Herath, H. M. M. T. B., et al.
Publicado: (2018)

Localized poïkiloderma
por: Kissou, Amina, et al.
Publicado: (2017)

Narrowband UVB phototherapy in pityriasis rosea
por: Jairath, Vijayeeta, et al.
Publicado: (2015)

A Familial Poikiloderma-Like Cutaneous Amyloidosis
por: Unni, Mahesh, et al.
Publicado: (2014)

Clinical approach to a child with poikiloderma: A case report
por: Shrestha, Samir, et al.
Publicado: (2021)

Macular amyloidosis presented as poikiloderma: a case report.
por: Kang, H. Y., et al.
Publicado: (2000)

Poikiloderma Vasculare Atrophicans Showing Features of Ashy Dermatosis in the Beginning
por: Jeon, Jiehyun, et al.
Publicado: (2015)

Poikiloderma Vasculare Atrophicans: A Distinct Clinical Entity?
por: Mahajan, Vikram K, et al.
Publicado: (2015)

Poikilodermatous changes on the forearms of a woman practicing aroma-therapy: extracervical poikiloderma of Civatte?()
por: Katoulis, Alexandros, et al.
Publicado: (2014)

Keloids: An Unwanted Spontaneity in Rubinstein-Taybi Syndrome
por: Shilpashree, P, et al.
Publicado: (2015)

The Role of Genetic Testing in Hereditary Poikiloderma: A Case Report
por: El-Heis, Sarah, et al.
Publicado: (2017)

Primary localized cutaneous amyloidosis with lichen and poikiloderma-like lesions and an excellent response to systemic acitretin
por: MA, Han, et al.
Publicado: (2016)

Lipedematous Scalp with Varied Presentations: A Case Series of Four Patients
por: Sahu, Priyadarshini, et al.
Publicado: (2019)

The Possible Role of Contact Sensitization to Fragrances and Preservatives in Poikiloderma of Civatte
por: Khunkhet, Saranya, et al.
Publicado: (2014)

Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
por: Goussot, Raphaëlle, et al.
Publicado: (2017)

A patient of Ebstein's anomaly associated with biventricular noncompaction presented with Wolf Parkinson White syndrome - A rare presentation
por: Patra, Soumya, et al.
Publicado: (2012)

Follicular Bronchiolitis: Two Cases with Varying Clinical and Radiological Presentation
por: Garg, Delyse, et al.
Publicado: (2020)

Granulomatous slack skin presenting as diffuse poikiloderma and necrotic ulcers, with features of granulomatous vasculitis and response to oral prednisone, acitretin, and oral psoralen plus ultraviolet light therapy—A case report
por: Puno, Maria Isabel Beatriz Lim, et al.
Publicado: (2017)

Diagnosis and Differential Diagnosis of Poikiloderma of Civatte: A Dermoscopy Cohort Study
por: Katoulis, Alexandros C., et al.
Publicado: (2023)

Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis: Hepatic disease in a child with a novel pathogenic variant of FAM111B
por: Dokic, Yelena, et al.
Publicado: (2020)

Poikiloderma With Neutropenia and Mastocytosis: A Case Report and a Review of Dermatological Signs
por: Piccolo, Vincenzo, et al.
Publicado: (2021)

A Case Series of Median Arcuate Ligament Syndrome With Varied Presentations
por: Abu-Hilal, Al-hakam H., et al.
Publicado: (2023)

A zebrafish model of Poikiloderma with Neutropenia recapitulates the human syndrome hallmarks and traces back neutropenia to the myeloid progenitor
por: Colombo, Elisa A., et al.
Publicado: (2015)

Varying Presentations of Multisystem Inflammatory Syndrome Temporarily Associated with COVID-19
por: Krikilion, Jasmina, et al.
Publicado: (2020)

Successful Treatment of Poikiloderma-Like Cutaneous Amyloidosis: A Case Report and Literature Review
por: Lin, Yi-Liang, et al.
Publicado: (2021)

Mutations in the ribosome biogenesis factor gene LTV1 are linked to LIPHAK syndrome, a novel poikiloderma-like disorder
por: Han, Ji Hoon, et al.
Publicado: (2022)

Lymphoma in HIV patients: Varied presentations
por: Saple, Dattatray G., et al.
Publicado: (2010)

An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report
por: Nallur Siddaraju, Maheshwari, et al.
Publicado: (2023)

Localized orbital amyloidosis – A varied presentation
por: Ramkumar, Akila V., et al.
Publicado: (2022)

Correlation of Vitamin D Levels with Pigmentation in Vitiligo Patients Treated with NBUVB Therapy
por: Sehrawat, Manu, et al.
Publicado: (2014)

Idiopathic Orofacial Granulomatosis with Varied Clinical Presentation
por: Ravindran, Rathy, et al.
Publicado: (2013)

Gossypiboma, Varied Presentations: A Report of Two Cases
por: Kohli, Supreethi, et al.
Publicado: (2013)

Varied presentations of pancreatic insulinoma: a case report
por: Nashidengo, Pueya Rashid, et al.
Publicado: (2022)

Case Report: Hereditary Fibrosing Poikiloderma With Tendon Contractures, Myopathy, and Pulmonary Fibrosis (POIKTMP) Presenting With Liver Cirrhosis and Steroid-Responsive Interstitial Pneumonia
por: Takimoto-Sato, Michiko, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_7clgbd3fbpm3ti3k017fslh2u1