Herlitz junctionele epidermolysis bullosa met bijzonder beloop

M. L. Castellanos Nuijts; H. H. Lemmink; F. G. Dikkers; J. M. Mandema; M. F. Jonkman

Herlitz junctionele epidermolysis bullosa met bijzonder beloop

Translated title of the contribution: Junctional epidermolysis bullosa type Herlitz: A case report with a special course

M. L. Castellanos Nuijts, H. H. Lemmink, F. G. Dikkers, J. M. Mandema, M. F. Jonkman

Research output: Contribution to journal › Article › Academic › peer-review

1 Citation (Scopus)

Abstract

Junctional epidermolysis bullosa type Herlitz (H-JEB) is a mechanobullous dermatosis with autosomal recessive heredity, clinically characterized by blisters, erosions and hypergranulation around nose, mouth, fingertips and subungually. H-JEB is usually fatal <2 years after birth. The described patient however did amazingly well considering the circumstances, but died at the age of 2 years and 9 months.

Translated title of the contribution	Junctional epidermolysis bullosa type Herlitz: A case report with a special course
Original language	Dutch
Pages (from-to)	17-18
Number of pages	2
Journal	Nederlands Tijdschrift voor Dermatologie en Venereologie
Volume	14
Issue number	1
Publication status	Published - Jan 2004

Cite this

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abstract = "Junctional epidermolysis bullosa type Herlitz (H-JEB) is a mechanobullous dermatosis with autosomal recessive heredity, clinically characterized by blisters, erosions and hypergranulation around nose, mouth, fingertips and subungually. H-JEB is usually fatal <2 years after birth. The described patient however did amazingly well considering the circumstances, but died at the age of 2 years and 9 months.",

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AU - Castellanos Nuijts, M. L.

AU - Lemmink, H. H.

AU - Dikkers, F. G.

AU - Mandema, J. M.

AU - Jonkman, M. F.

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AB - Junctional epidermolysis bullosa type Herlitz (H-JEB) is a mechanobullous dermatosis with autosomal recessive heredity, clinically characterized by blisters, erosions and hypergranulation around nose, mouth, fingertips and subungually. H-JEB is usually fatal <2 years after birth. The described patient however did amazingly well considering the circumstances, but died at the age of 2 years and 9 months.

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SN - 0925-8604

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JF - Nederlands Tijdschrift voor Dermatologie en Venereologie

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ER -

Herlitz junctionele epidermolysis bullosa met bijzonder beloop

Abstract

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