Cover Image

Lipoid proteinosis: different clinical features in two siblings

Saved in:

Bibliographic Details
Main Authors:	Katarzyna Łuczak (Author), Elżbieta Wojtowicz-Prus (Author), Robert Śmigiel (Author), Katarzyna Wertheim-Tysarowska (Author), Sylwia Radomska (Author), Jacek Podolski (Author), Jolanta Węgłowska (Author)
Format:	Book
Published:	Termedia Publishing House, 2019-12-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Lipoid proteinosis in two siblings
by: Behera Samira Kumar, et al.
Published: (2006)

Lipoid proteinosis: Curious case of two siblings!
by: Pooja Agarwal, et al.
Published: (2020)

Lipoid proteinosis (Urbach-Wiethe disease) in two siblings
by: Rekha Thaddanee, et al.
Published: (2014)

Lipoid proteinosis
by: Sen Sumit, et al.
Published: (2006)

Lipoid proteinosis
by: Mukhija Pooja, et al.
Published: (2006)

Acitretin Treatment for Lipoid Proteinosis
by: Özgür Gündüz, et al.
Published: (2012)

Lipoid proteinosis: A review with two case reports
by: Vishal Kabre, et al.
Published: (2015)

Urbach-Wiethe disease (lipoid proteinosis)
by: Ulku Kucuk, et al.
Published: (2012)

Lipoid proteinosis: A rare case revisited
by: Arun Achar, et al.
Published: (2023)

Association Between Lipoid Proteinosis And Coeliac Disease
by: Layla Bendaoud, et al.
Published: (2023)

Lipoid proteinosis: A series of three cases
by: Astha Sharma, et al.
Published: (2018)

Lipoid proteinosis: A rare clinical entity
by: Goyal Puja, et al.
Published: (2012)

Lipoid Proteinosis: A Rare Encounter in Dental Office
by: Prasannasrinivas Deshpande, et al.
Published: (2015)

Lipoid proteinosis: Histopathological characterization of early papulovesicular lesions
by: Rameshwar Gutte, et al.
Published: (2012)

An unusual case of erythropoietic protoporphyria mimicking lipoid proteinosis
by: Sarabjit Kaur, et al.
Published: (2019)

Lipoid proteinosis in a six-year-old child
by: Surajit Nayak, et al.
Published: (2012)

Successful use of acitretin in an indian child with lipoid proteinosis
by: Shraddha P Kote, et al.
Published: (2022)

Ultrastructural aspects of the skin in lipoid proteinosis (Urbach-Wiethe disease),
by: Hiram Larangeira de Almeida Jr, et al.
Published: (2022)

Intra-familial variability of lipoid proteinosis: An Indian case series
by: Kriti Lohia, et al.
Published: (2021)

Lipoid Proteinosis: A Rare Case Report and Review of Literature
by: Damini Verma, et al.
Published: (2024)

Urbach-Weithe disease (lipoid proteinosis): A classical presentation
by: Ankita Sangwan, et al.
Published: (2016)

Molecular and neurological characterizations of three Saudi families with lipoid proteinosis
by: Al-Fakey Yasser H, et al.
Published: (2011)

Clinical and molecular characterization of lipoid proteinosis in three Indian families
by: Sahana M Srinivas, et al.
Published: (2020)

Oral manifestations of lipoid proteinosis: A case report and literature review
by: S.M. Ravi Prakash, et al.
Published: (2013)

Lipoid Proteinosis with Esotropia: Report of a Rare Case and Dermoscopic Findings
by: Hera Tabassum, et al.
Published: (2020)

Lipoid Proteinosis: A Previously Unrecognized Mutation and Therapeutic Response to Acitretin
by: Claudia Carnevale, et al.
Published: (2017)

Oral findings in a child with lipoid proteinosis: A case report and review
by: S Mainali, et al.
Published: (2011)

Extracellular matrix protein 1 gene mutation in turkish patients with lipoid proteinosis
by: Selma Bakar Dertlioğlu, et al.
Published: (2019)

Lipoid Proteinosis treated as post acne scars - A clinical diagnostic error
by: Shagufta Rather, et al.
Published: (2015)

A rare case report of lipoid proteinosis with distichiasis and trichomegaly: An interesting entity
by: H Bangaru, et al.
Published: (2024)

A Sporadic Family of Lipoid Proteinosis with Novel ECM1 Gene Mutations
by: Liu YL, et al.
Published: (2024)

Lipoid proteinosis with oral manifestation in a geriatric patient: A unique case report
by: Jayachandran Sadaksharam, et al.
Published: (2015)

Novel compound heterozygous mutations of ECM1 in a Chinese family with lipoid proteinosis
by: Wei Wu, et al.
Published: (2019)

Oral Manifestations and Dental Management Considerations of Lipoid Proteinosis: A Case Report and Review of Literature
by: Fatemeh Jahanimoghadam, et al.
Published: (2022)

Lipoid proteinosis coexisting with rare psychiatric manifestations: a case report with a review of literature
by: Kritika Gupta, et al.
Published: (2023)

Cryosurgery (N2O) application to remove lip lesions of lipoid proteinosis syndrome: a case report
by: Amir Mansour Shirani
Published: (2008)

Identification of a Novel Mutation of Extracellular Matrix Protein 1 Gene in a Chinese Family with Lipoid Proteinosis
by: Xu M, et al.
Published: (2023)

Molecular analysis of lipoid proteinosis: identification of a novel nonsense mutation in the <it>ECM1 </it>gene in a Pakistani family
by: Naeem Muhammad, et al.
Published: (2011)

Lipoid Proteinosis Due to Homozygous Deletion Mutation (c.735delTG) in the ECM1 Gene Presents with Seizures and Hoarseness but No Skin Involvement
by: Hassan Vahidnezhad, et al.
Published: (2020)

Epidermolysis bullosa - pęcherzowe oddzielanie się naskórka. Etiopatogeneza, dziedziczenie, diagnostyka, leczenie
by: Katarzyna Wertheim-Tysarowska, et al.
Published: (2014)