2004
DOI: 10.1038/sj.eye.6700686
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Eye changes in a patient with lamellar ichthyosis and toe pseudoainhum

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Cited by 9 publications
(11 citation statements)
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“…Severe meibomian gland dysfunction (MGD) has been reported to occur in a 41-year-old man with LI15 and a 3-year-old girl as well as her father with ichthyosis follicularis 17. The girl also had madarosis and loss of eyebrows since birth.…”
Section: Ophthalmic Featuresmentioning
confidence: 99%
“…Severe meibomian gland dysfunction (MGD) has been reported to occur in a 41-year-old man with LI15 and a 3-year-old girl as well as her father with ichthyosis follicularis 17. The girl also had madarosis and loss of eyebrows since birth.…”
Section: Ophthalmic Featuresmentioning
confidence: 99%
“…2,29,42 This report describes a case of pseudoainhum presenting with properties characteristic of TSC. This association, which has not been previously Disorders of abnormal keratinization Psoriasis [15][16][17] Pityriasis rubra pilaris 18 Porokeratosis of Mibelli 19 Congenital linear porokeratosis 20 Focal acral hyperkeratosis and angiodysplasia 21 Lamellar ichthyosis [22][23][24] Keratosis palmoplantaris with polydactyly and eosinophilia 25 Keratoma hereditarium dissipatum palmare et plantare (Buschke-Fischer-Brauer) 26 Keratoderma hereditarium mutilans (Vohwinkel) [27][28][29][30][31][32] Progressive symmetric erythrokeratoderma (PSEK) 4 Keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK) 5 Keratosis palmoplantaris transgradiens of Siemens (mal de Meleda) 6,33 Clouston's syndrome 34 Ectodermal dysplasia syndrome (with cataracts, alopecia, sclerodactyly) 35 Papillon-Lefevre syndrome 36 Loricrin keratoderma 32 Metabolic and neurologic diseases Isolated polyneuropathy 37 Gout disease 38 Alcohol-toxic polyneuropathy 9 Erythropoietic protoporphyria 11 Plica neuropathica, hair matting, schizophrenia 10 Reynolds syndrome and breast cancer 14 Connective tissue diseases Rheumatoid arthritis 39 Discoid lupus erythematosus 40 Localized scleroderma 41,42 Bullous disease Hereditary bullous acrokeratotic poikiloderma of Wea...…”
Section: Discussionmentioning
confidence: 76%
“…Family members should also be carefully examined for co‐morbid syndromes and for pseudo‐ainhum itself. Other organ systems may be affected and thus should not be overlooked 39 . A comprehensive and careful review and examination is required.…”
Section: Management and Prognosismentioning
confidence: 99%
“…Other organ systems may be affected and thus should not be overlooked. 39 A comprehensive and careful review and examination is required.…”
Section: Management and Prognosismentioning
confidence: 99%