نتایج جستجو برای: oculocutaneous albinism

تعداد نتایج: 7152  

Journal: :Clinical and experimental dermatology 2014
S A Shah S U Din N Raheem S Daud J Mubeen A Nadeem M Tayyab D M Baloch M E Babar J Ahmad

The TYR gene (MIM #6069333) is located at position 11q14.3 on the human chromosome, and encodes tyrosinase, which is expressed in melanocytes and controls the biosynthesis of melanin. Most TYR mutations eliminate the activity of tyrosinase, preventing melanocytes from producing any melanin throughout life. People with this form of albinism have white hair, light-coloured eyes and very pale skin...

2017
Rosario Peralta Emilia Cohen Sabban Paula Friedman Carolina Marcucci Luis A. Bollea Garlatti Gastón Galimberti Horacio Cabo

Albino patients are at great risk for developing cutaneous neoplasms, including melanomas. In this paper we describe the dermatoscopic findings of nevi in two patients with oculocutaneous albinism type Ia (OCA-Ia) highlighting that they manifest a vascular pattern similar to that described for amelanotic melanoma. We propose managing these patients with dermoscopy, using the comparative approac...

2014
Murat Elevli Halil Uğur Hatipoğlu Mahmut Civilibal Nilgün Selçuk Duru Tiraje Celkan

To the Editor, Chediak-Higashi syndrome (CHS) is a rare, autosomal recessive inherited disorder characterized by variable degrees of oculocutaneous albinism, severe immune deficiency and unassociated lymphoproliferative syndrome, and intracytoplasmic giant granules in leukocytes, monocytes, platelets, melanocytes, and erythroid precursors [1,2,3,4,5]. CHS is caused by mutations in the lysosomal...

2017
Yaqiong Jin Li Zhang Senfen Wang Feng Chen Yang Gu Enyu Hong Yongbo Yu Xin Ni Yongli Guo Tieliu Shi Zigang Xu

Chediak-Higashi syndrome (CHS) is a rare autosomal recessive disease characterized by varying degrees of oculocutaneous albinism, recurrent infections, and a mild bleeding tendency, with late neurologic dysfunction. This syndrome is molecularly characterized by pathognomonic mutations in the LYST (lysosomal trafficking regulator). Using whole genome sequencing (WGS) we attempted to identify nov...

Journal: :Investigative ophthalmology & visual science 2017
Ryoko Oki Kisaburo Yamada Satoko Nakano Kenichi Kimoto Ken Yamamoto Hiroyuki Kondo Toshiaki Kubota

Purpose We report the clinical characteristics of a Japanese family with autosomal dominant oculocutaneous albinism and a SLC45A2 gene mutation. Methods A total of 16 members of a Japanese family with general hypopigmentation and foveal hypoplasia underwent detailed clinical examinations. We evaluated the severity of foveal hypoplasia using spectral-domain optical coherence tomography (SD-OCT...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید