نتایج جستجو برای: lipoid proteinosis

تعداد نتایج: 15341  

Journal: :Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale 2006
S Di Giandomenico R Masi D Cassandrini M El-Hachem R De Vito C Bruno F M Santorelli

Lipoid proteinosis is a rare autosomal recessive disorder, characterized histologically by infiltration of periodic acid Schiff-positive hyaline material into the skin, upper aerodigestive tract, and internal organs. Classical clinical features include skin scarring, beaded eyelid papules, and laryngeal infiltration leading to hoarseness. Moreover, the infiltrates in the tongue and its frenulum...

2011
Muhammad Nasir Amir Latif Muhammad Ajmal Reem Qamar Muhammad Naeem Abdul Hameed

UNLABELLED Lipoid proteinosis is a rare autosomal recessive disease characterized by cutaneous and mucosal lesions and hoarseness appearing in early childhood that is caused by homozygous or compound heterozygous mutations in the ECM1 gene located on chromosome 1q21. The aim of the study was to investigate the molecular genetic defect underlying lipoid proteinosis in a consanguineous Pakistani ...

Journal: :The British journal of ophthalmology 1979
V Feiler-Ofry A Lewy L Regenbogen D Hanau M B Katznelson V Godel

A Jewish-Iranian family suffered from lipoid proteinosis. The 8 affected siblings were from consanguineous matings and presented a wide range of phenotypic expressions. Minimal manifestations in 2 heterozygote carriers and the possibility of autosomal recessive inheritance are discussed.

Journal: :British Journal of Anaesthesia 1989

Journal: :Ear, Nose & Throat Journal 2015

Journal: :Indian Journal of Dermatology 2006

Journal: :British Journal of Ophthalmology 1979

Journal: :Case Reports in Dermatological Medicine 2012

Journal: :Journal of Dr. NTR University of Health Sciences 2017

Journal: :The European respiratory journal 1996
K Sato H Takahashi H Amano T Uekusa T Dambara S Kira

We describe an 18 year old male with pulmonary interstitial and intra-alveolar cholesterol granulomas (PICG), which developed to severe respiratory failure over 15 yrs. The histological diagnosis was made on the basis of open lung biopsy findings at the age of 3 yrs and autopsy at 18 yrs of age. Although the pathological features of the lung were similar to that of paediatric patients with lipo...

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