نتایج جستجو برای: lamellar ichthyosis

تعداد نتایج: 8730  

Journal: :The Journal of allergy and clinical immunology 2017
Amy S Paller Yael Renert-Yuval Maria Suprun Hitokazu Esaki Margeaux Oliva Thy Nhat Huynh Benjamin Ungar Norma Kunjravia Rivka Friedland Xiangyu Peng Xiuzhong Zheng Yeriel D Estrada James G Krueger Keith A Choate Mayte Suárez-Fariñas Emma Guttman-Yassky

BACKGROUND The ichthyoses are rare genetic disorders associated with generalized scaling, erythema, and epidermal barrier impairment. Pathogenesis-based therapy is largely lacking because the underlying molecular basis is poorly understood. OBJECTIVE We sought to characterize molecularly cutaneous inflammation and its correlation with clinical and barrier characteristics. METHODS We analyze...

Journal: :Proceedings of the Royal Society of Medicine 1973

Journal: :Journal of Postgraduate Medicine 2007

Journal: :Archives of disease in childhood 1988
K Lui C Commens R Choong R Jaworski

Two neonates with acute infantile cerebral Gaucher's disease had prominent collodion skin. Ichthyosis has been described in some cases of metabolic lipid disorders, however, this is the first report of the association of lamellar desquamation of the newborn (collodion baby) with Gaucher's disease.

2010
Agneta Gånemo

Congenital ichthyosis encompasses a large group of keratinizing disorders with widespread scaling and a variable degree of erythema. Little is known about the quality of life in children with congenital ichthyosis and the impact of the disease on their family. Fifteen children aged 5-16 years with lamellar ichthyosis, Netherton's syndrome, epidermolytic hyperkeratosis or Harlequin ichthyosis, w...

Journal: :Indian Journal of Dermatology, Venereology and Leprology 2017

Journal: :Acta Dermatovenerologica Alpina Pannonica et Adriatica 2016

Journal: :Journal of dermatological science 2006
Masashi Akiyama

Autosomal recessive congenital ichthyoses (ARCI) include several severe subtypes including harlequin ichthyosis (HI), lamellar ichthyosis and non-bullous congenital ichthyosiform erythroderma. Patients with these severe types of ichthyoses frequently show severe hyperkeratosis and scales over a large part of the body surface form birth and their quality of life is often severely affected. Recen...

2016
Kruti Parikh Kanwaljit Brar Jaimie B. Glick Alexandra Flamm Sharon A. Glick

ABCA12: adenosine triphosphate binding cassette A12 HI: harlequin ichthyosis NICU: neonatal intensive care unit INTRODUCTION Harlequin ichthyosis (HI) is a rare autosomal recessive congenital ichthyosis associated with mutations in the keratinocyte lipid transporter adenosine triphosphate binding cassette A12 (ABCA12), leading to disruption in lipid and protease transport into lamellar granules...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید