Lipoid Proteinosis with Homozygous ECM1 c.507del Variant and Functionally Significant Eyelid Involvement: A Case Report. [PDF]
Hu L, Xu Y, Zhao W.
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A Rare Ocular Manifestation of Lipoid Proteinosis. [PDF]
Ng XG, Mpt J, Ang EL.
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Early diagnosis of a case of lipoid proteinosis due to a previously undescribed deletion in ECM1 gene. [PDF]
Mansilla-Polo M +4 more
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Lipoid Proteinosis with Esotropia: Report of a Rare Case and Dermoscopic Findings. [PDF]
Tabassum H +5 more
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Lipoid Proteinosis-An Unusual Cause of Hoarseness of Voice in a Child: Case Report. [PDF]
Ghosh A, Kumar M, Satija B, Nangia A.
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Genotype-Phenotype Correlation in Lipoid Proteinosis: 15 Cases from Turkiye. [PDF]
Dinçsoy Bir F +10 more
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A Rare Case of Lipoid Proteinosis in a Patient Presenting With Seizures: A Case Report and Literature Review. [PDF]
Patil C +4 more
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Lipoid Proteinosis: A Rare Case Report and Review of Literature. [PDF]
Verma D +4 more
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Lipoid proteinosis: A rare genodermatosis with multisystemic manifestations-A case report. [PDF]
Hashmi FN +7 more
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A Sporadic Family of Lipoid Proteinosis with Novel ECM1 Gene Mutations. [PDF]
Liu YL, Zhang ZY, Chen XM.
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