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The New England journal of medicine, 1972
Biopsy specimens from patients with lamellar ichthyosis were studied by histologic, enzyme histochemical, and electron microscopic methods. Routine sections were not diagnostic, showing hyperkeratosis, normal or thickened granular zone, and acanthosis and papillomatosis.
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Biopsy specimens from patients with lamellar ichthyosis were studied by histologic, enzyme histochemical, and electron microscopic methods. Routine sections were not diagnostic, showing hyperkeratosis, normal or thickened granular zone, and acanthosis and papillomatosis.
+5 more sources
Autosomal dominant lamellar ichthyosis
Clinical Genetics, 1986Five members of two generations of one family were affected with lamellar ichthyosis, suggesting autosomal dominant transmission. The clinical and histopathological characteristics of the cases described here are similar to those reported by Traupe et al.
J, Toribio +4 more
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ICHTHYOSIS–LAMELLAR EXFOLIATIVE TYPE
International Journal of Dermatology, 1963Summary and ConclusionsNine cases (six males and three females) of ichthyosis of the lamellar exfoliative type occurred among 22 offspring in three related families of German origin. All six parents have a common ancestor and are first cousins or fourth cousins once removed. Inheritance is by an autosomal recessive gene with 100%penetrance.
T E, NIX, H W, KLOEPFER, V J, DERBES
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Cicatricial Ectropion in Lamellar Ichthyosis
Ophthalmic Plastic & Reconstructive Surgery, 1990A 35-year-old woman presented with bilateral lower lid ectropion associated with lamellar ichthyosis. She was successfully treated with postauricular skin grafts and horizontal lid shortenings. This report reviews the literature on the surgical management of this condition and suggests several modifications to prevent recurrence.
R P, Doss, H, Conn, D P, Tenzel
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Lamellar Ichthyosis in a Recluse
International Journal of Dermatology, 1983Un cas chez un homme de 70 ans canadien francais, ayant vecu reclu en raison de son apparence ...
J E, Adam, L, Weatherhead
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Archives of Dermatology, 1968
The clinical and microscopic data from previously published cases of lamellar exfoliation of the newborn (collodion baby) have been summarized, and four new cases of the entity with follow-up observations and kinetic studies have been presented. The clinical, histopathological, genetic, and kinetic features of our cases after desquamation of the ...
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The clinical and microscopic data from previously published cases of lamellar exfoliation of the newborn (collodion baby) have been summarized, and four new cases of the entity with follow-up observations and kinetic studies have been presented. The clinical, histopathological, genetic, and kinetic features of our cases after desquamation of the ...
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Collodion baby and lamellar ichthyosis
Journal of Cutaneous Pathology, 1998It is important to differentiate the collodion baby from harlequin ichthyosis as the latter rarely survives past the first few days of life. Occasionally, babies share features of both disorders and defy a clinical diagnosis. We recently encountered such a baby who initially presented with harlequin‐like features, but evolved into lamellar ichthyosis ...
B, Sandler, K, Hashimoto
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Cyclosporine in lamellar ichthyosis.
Archives of dermatology, 1989In an open trial, five patients with lamellar ichthyosis showed no response to four weeks of treatment with oral cyclosporine (cyclosporine A) (6 mg/kg/d). Histologic examination of lamellar ichthyosis revealed hyperkeratosis; psoriasiform acanthosis; dilated, tortuous capillaries; and a slight perivascular lymphocytic infiltrate.
V C, Ho +5 more
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Lamellar ichthyosis with bilateral ectropion
Nigerian Journal of Ophthalmology, 2015Lamellar ichthyosis is a rare congenital disorder with ocular manifestation resulting from the cicatrization of anterior lamella of eyelids. Early diagnosis and management of ectropion can prevent the most severe complications such as severe dry eyes, corneal perforation, and possible loss of the eye.
Jain, Gunjan +4 more
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Pediatrics In Review, 1981
Congenital ichthyoses represent a heterogeneous group of rare skin diseases. The disorders are heritable and have in common a varying degree of hyperkeratosis. During the years there has been much confusion regarding the classification of the ichthyoses.
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Congenital ichthyoses represent a heterogeneous group of rare skin diseases. The disorders are heritable and have in common a varying degree of hyperkeratosis. During the years there has been much confusion regarding the classification of the ichthyoses.
openaire +1 more source