Hyperkeratosis Lenticularis Perstans

Bean, Samuel F.

doi:10.1001/archderm.1969.01610240063011

Cited by 20 publications

(1 citation statement)

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“…Especially, I think of hyperkeratosis lenticularis perstans which was described by F leg el in 1958. 11 years later, Bean [1969] published the first family. This and other studies have shown that this disturbance of keratinization has an autosomal dominant inheritance.…”

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confidence: 99%

Genetics and Dermatology

Schnyder¹

1975

Dermatology

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An attempt has been made to show and discuss today’s problems of geno-dermatology, mentioning the important groups of the heterogenous diseases and enzyme defects which are coupled with the skin diseases. Moreover, the chromosomes breakage syndromes are reviewed. To a great extent, these problems are of theoretical interest, but the genetic counselling is on the increase and already plays an important part in the daily routine of the large hospitals.

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confidence: 99%

Genetics and Dermatology

Schnyder¹

1975

Dermatology

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Unilateral Asymptomatic Progressive Eruption of Hyperkeratotic Papules

2019

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Inherited Disorders of Cornification

Oji

Metze

Traupe

2016

Rook's Textbook of Dermatology, Ninth Edition

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The majority of keratinization disorders are referred to as Mendelian disorders of cornification. This is a very broad group, clinically characterized by hyperkeratosis or visible scaling or both. This chapter deals with the ichthyoses, palmoplantar keratodermas (PPKs) and miscellaneous cornification disorders such as porokeratoses. It is aimed primarily at dermatologists and physician scientists who have to make a clinical diagnosis and provide adequate management for their patients. Therefore a nosology and classification scheme has been chosen that is based on clinicogenetic and morphological features. Clinical diagnoses are then discussed with their molecular pathology. Part of the chapter addresses the management of congenital ichthyoses. Various tables provide an overview on clinical and/or pathophysiologically related groups of diseases. Finally, several cornification disorders are discussed that do not have a genetic basis, but are acquired or are of unknown aetiology (e.g. acquired ichthyoses/PPKs or perforating keratotic disorders).

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Hyperkeratosis Lenticularis Perstans

Cited by 20 publications

References 3 publications

Genetics and Dermatology

Genetics and Dermatology

Unilateral Asymptomatic Progressive Eruption of Hyperkeratotic Papules

Inherited Disorders of Cornification

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