نتایج جستجو برای: pigmentation disorder

تعداد نتایج: 606376  

Journal: :iranian journal of child neurology 0
seyed ebrahim mansouri nejad 1. department of pediatric neurology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhahd, iran mohammad javad yazdan panah 2. research center for cutaneous leishmaniasis, mashhad university of medical sciences, mashhahd, iran 3.department of dermatology, mashhad university of medical sciences, mashhahd, iran naser tayyebi meibodi 2. research center for cutaneous leishmaniasis, mashhad university of medical sciences, mashhahd, iran 4. department of pathology, mashhad university of medical sciences, mashhahd, iran farah ashrafzadeh* 1. department of pediatric neurology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhahd, iran mehran beiraghi toosi 1. department of pediatric neurology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhahd, iran javad akhondian 1. department of pediatric neurology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhahd, iran

how to cite this article: mansouri nejad se, yazdan panah mj, tayyebi meibodi n, ashrafzadeh f, akhondian j, beiraghi toosi m, eslamieh h. griscelli syndrome: a case report. iran j child neurol. 2014 autumn;8(4): 72-75. objective griscelli syndrome (gs) is a rare autosomal recessive immune deficiency disorder that presents with pigmentary dilution of the skin and hair, recurrent skin and pulmon...

Background: Segmental pigmentation disorder (SegPD) is a rare type of cutaneous dyspigmentation. This hereditary disorder, first described some 20 years ago, is characterized by hypo and hyperpigmented patches on the trunk, extremities and less likely on the face and neck. These lesions are considered as a type of checkerboard pattern. Case Presentation: Herein, we present a 26-year-old male...

انصاری, شهلا, ساده‌دل, روزبه , هاشمی, مهدی, آهنچی, نوید ,

Fanconi anemia is the most prevalent form of inherited aplastic anemia which is characterized by progressive bone marrow failure, congenital anomalies and cancer susceptibility. Common anomalies are skeletal abnormalities, skin pigmentation disorder, short stature, head abnormalities, kidney and gonad disorders respectively. Complications of fanconi anemia include: leukemia due to defective DNA...

Journal: :Journal of drugs in dermatology : JDD 2012
Lisa Zaleski Sabrina Fabi Mitchel P Goldman

Melasma is a complex multifactorial disorder whose pathogenesis is not well understood. In addition to increased pigmentation, increased vascularity associated with pigmentation is present. A variety of topical treatments targeting pigmentation are available with temporary improvement of mainly the epidermal components of melasma. Intense pulsed light (IPL) is a broadband light source that can ...

Journal: :Clinics in dermatology 2005
Thierry Passeron Frédéric Mantoux Jean-Paul Ortonne

More than 127 loci are actually known to affect pigmentation in mouse when they are mutated. From embryogenesis to transfer of melanin to the keratinocytes or melanocytes survival, any defect is able to alter the pigmentation process. Many gene mutations are now described, but the function of their product protein and their implication in melanogenesis are only partially understood. Each geneti...

2010
THOMAS B. FITZPATRICK

One of the most striking phenomena in human oncology is the transformation of the normal skin color to an intense blue-gray pigmentation. This occurs as a complication of malignant melanoma. In the recent literature, several excellent examples of this type of pigmentation have been reported in patients with malignant melanoma. In this paper we report on another patient with generalized melanin ...

Journal: :Cutis 2011
Payman Kosari Kristen M Kelly

Laugier-Hunziker syndrome is a rare mucocutaneous pigmentary disorder. It is considered benign, but other mucocutaneous pigmentation disorders are in the differential diagnosis and should be ruled out. This report describes a woman with pigmentation of the labial mucosa of the lower lip who was successfully treated with a Q-switched 532-nm laser.

Journal: :Journal of Investigative Dermatology 2023

Skin pigmentation disorders pose serious dermatological concerns and bring immense psychological burdens to individuals suffering from them. Vitiligo is one such disorder resistant various conventional treatments. It caused by an autoimmune-mediated destruction of epidermal melanocytes, resulting in focal loss skin pigmentation. The hair follicle bulge holds a stem cell (SC) population directly...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید