نتایج جستجو برای: hermansky

تعداد نتایج: 390  

Journal: :Tuberkuloz ve toraks 2011
Aydın Ciledağ Burcu Cirit Koçer Nurdan Köktürk Akın Kaya Gökhan Celik Numan Numanoğlu

Hermansky-Pudlak syndrome is a rare disease characterized by bleeding diathesis, oculocutaneous albinism and lysosomal ceroid lipofuscin pigment deposits. Pulmonary fibrosis may also accompany with the disease. A 48-year-old male patient with a diagnosis of Hermansky-Pudlak syndrome admitted with dyspnea. A thorax computed tomography revealed bilateral diffuse interlobular septal thickness whic...

2010
Abbas Bagheri Asieh Abdollahi

PURPOSE To report a case of Hermansky-Pudlak syndrome. CASE REPORT A seven-year-old boy presented with marked generalized hypopigmentation, ocular exodeviation and nystagmus. He had history of easy bruising. Examination revealed green irides with marked transillumination, hypopigmented fundi and foveal hypoplasia. Further investigations disclosed platelet storage defect with adenosine diphosp...

2012
Hilary Denis Solomons

Validation of a method of blood pressure measurement for a study of hypertension in a black African population. Cahiers d'études recherches francophones/santé vasculaire chez l'adulte en milieu rural à Thiadiaye. The prevalence of hyperten-sion and its relationship with obesity: results from a national blood pressure survey in Eritrea. Faciès de l'hypertension artérielle en milieu professionnel...

2017
Natalio J. Izquierdo Alejandro Acosta Pedro J. Dávila

Introduction: The Hermansky-Pudlak syndrome is an autosomal recessive disease characterized by oculo cutaneous albinism, a bleeding diathesis and lysosomal accumulation of ceroid lipofuscin. Objectives: To do a comprehensive literature review of the clinicopathological findings in patients with the Hermasnky-Pudlak syndrome, its diagnosis, management, and treatment. Methods: A literature review...

Journal: :Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2015
Mazhar Ishaq Muhammad Khizar Niazi Muhammad Saim Khan Yasser Nadeem

Albinism is an inherited abnormality of melanin synthesis with incidence of one per 20,000 births. Its clinical manifestations are related to the reduction or absence of pigmentation in the visual system and/or the skin and teguments. The clinical spectrum of Oculocutaneous Albinism (OCA) has four types ranging from OCA 1 - 4, of which OCA 1, A-1 is the most severe form. Partial cutaneous albin...

Journal: :Blood 2015
Anish Sharda Sarah H Kim Reema Jasuja Srila Gopal Robert Flaumenhaft Barbara C Furie Bruce Furie

Protein disulfide isomerase (PDI), secreted from platelets and endothelial cells after injury, is required for thrombus formation. The effect of platelet and endothelial cell granule contents on PDI-mediated thrombus formation was studied by intravital microscopy using a mouse model of Hermansky-Pudlak syndrome in which platelet dense granules are absent. Platelet deposition and fibrin generati...

Journal: :Clinics in Chest Medicine 2016

Journal: :بینا 0
عباس باقری a bagheri ophthalmic research center, shahid beheshti university of medical sciences, tehran, iranتهران- پاسداران- خیابان امیر ابراهیمی- نبش بوستان نهم- پلاک 5- مرکز تحقیقات چشم آسیه عبداللهی a abdolahi ophthalmic research center, shahid beheshti university of medical sciences, tehran, iranتهران- پاسداران- خیابان امیر ابراهیمی- نبش بوستان نهم- پلاک 5- مرکز تحقیقات چشم

purpose: to report a case of hermansky-pudlak syndrome (hps). case report: a 7-year-old boy presented with marked generalized hypopigmentation, eye deviation and nystagmus. in addition he had history of easy bruising. visual acuity was 20/200. he had markedly translucent green irides, hypermetropic astigmatism, horizontal nystagmus and marked exotropia. funduscopy revealed a hypopigmented retin...

Journal: :The Journal of the Association of Physicians of India 2009
Tiyas Sen Jai Mullerpattan Dipika Agarwal Deepak Naphde Ramesh Deshpande Ashok A Mahashur

We present a rare disease condition Hermansky-Pudlak syndrome in a 33-year-old male. He was born of a consanguineous marriage, had occulo-cutaneous albinism, nystagmus, decreased visual acuity, refractory errors, pulmonary fibrosis and granulomatous inflammation of the colon. In spite of all the classical features of this genetic disorder he was labeled to have disseminated tuberculous infectio...

2017
Naoki Oiso Akira Kawada

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