نتایج جستجو برای: Meleda disease

تعداد نتایج: 1490125  

Journal: :Acta dermatovenerologica Croatica : ADC 2016
Emre Adıgüzel Emine Yüksel İsmail Safaz Arif Kenan Tan

Mal de Meleda is a rare autosomal recessive skin disease which is known as keratoderma palmoplantaris transgradiens. Here we report a case of Mal de Meleda who had skin lesions in the residual limb and pseudoainhum in the thigh after traumatic lower leg amputation. A 71-year-old female was admitted to our tertiary hospital for prosthetic rehabilitation. On the physical examination, thickening o...

Journal: :The Journal of investigative dermatology 2003
Guofang Hu Mehmet Yildirim Vahide Baysal Ozlem Yerebakan Ertan Yilmaz H Serhat Inaloz Amalia Martinez-Mir Angela M Christiano Julide Tok Celebi

Mal de Meleda is a rare form of palmoplantar keratoderma, and recently mutations in the ARS (component) B gene have been identified in families with this disease. We identified a recurrent nonsense mutation, R96X, in four families of Turkish descent. In this report, we demonstrate that these families share a common ancestral haplotype at the mal de Meleda locus, suggesting a founder effect.

Journal: :Vestnik dermatologii i venerologii 2020

Journal: :Acta medico-historica adriatica : AMHA 2010
Marija Gjurasić

Nowadays, hereditary diseases are viewed through molecular mechanisms, and one of them, which keeps occurring rather frequently in medical publications, has been named after the Island of Mljet. The world first learned about mal de Meleda from a Dubrovnik physician Luka Stulli in 1826. He described it in a number of his island patients as a non-contagious hereditary skin disease, and named it m...

Journal: :Acta dermatovenerologica Croatica : ADC 2014
Ana Bakija-Konsuo

Meleda disease is an indigenous dermatological disease classified as a hereditary palmoplantar keratoderma. The disease was first described on the island of Mljet, Croatia, by Luko Stulli in 1826. We present a historical review of the literature data throughout the centuries till today. Recently, the gene responsible for the disease has been identified on chromosome 8qter within the cluster of ...

Journal: :European Journal of Human Genetics 1998

Journal: :Archives of dermatology 2000
B Bouadjar S Benmazouzia J F Prud'homme S Cure J Fischer

BACKGROUND Mal de Meleda (MIM 248300), also referred to as keratosis palmoplantaris transgrediens of Siemens, is a rare autosomal recessive skin disorder with a prevalence in the general population of 1 in 100,000. The main clinical characteristics are transgressive palmoplantar keratoderma, hyperhidrosis, and perioral erythema, but there are also associated features such as brachydactyly, nail...

2010
Mbarka Bchetnia Ahlem Merdassi Cherine Charfeddine Fatma Mgaieth Selma Kassar Farah Ouechtati Ibtissem Chouchene Hamouda Boussen Mourad Mokni Amel Dhahri-Ben Osman Med Samir Boubaker Sonia Abdelhak Leila Elmatri

INTRODUCTION Mal de Meleda is a rare form of palmoplantar keratoderma, with autosomal recessive transmission. It is characterized by diffuse erythema and hyperkeratosis of the palms and soles. Recently, mutations in the ARS (component B) gene (ARS, MIM: 606119) on chromosome 8q24.3 have been identified in families with this disorder. Congenital cataract is a visual disease that may interfere wi...

Journal: :Journal of Investigative Dermatology 2003

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