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Self-improving dystrophic epidermolysis bullosa

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Disease definition

A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized blistering at birth that usually regresses within the first 6 to 24 months of life.

ORPHA:79411

Classification level: Disorder

Synonym(s):
  • Self-improving DEB
  • Transient bullous dermolysis of the newborn

Source: PubMed ID 32017015

Prevalence: <1 / 1 000 000

Inheritance: Autosomal dominant, Autosomal recessive

Age of onset: Infancy, Neonatal

ICD-10: Q81.2

ICD-11: EC32

OMIM: 131705

UMLS: C1851573

MeSH: C536979

GARD: 10010

Summary
Epidemiology

Prevalence is unknown. To date, 52 cases have been reported.

Clinical description

The disease usually manifests at birth, or soon after. Skin blisters generally affect the whole body. Blisters can also affect the oral cavity. Healing of blisters is associated with mild, mostly atrophic, scarring and milia formation. Disease activity usually ceases within the first 6 to 24 months of life, although there are a few cases with continued blistering past age 3 years. Nail dystrophy and some degree of skin fragility can persist in adulthood. Ultrastructurally, the presence in basal keratinocytes of peculiar cytoplasmic inclusions, known as stellate bodies, filled with unsecreted procollagen VII, is typical of the disease.

Etiology

The disorder is caused by mutations within the type VII collagen gene (COL7A1; 3p21.31). Mutations in this gene lead to reduced amounts or an alteration in function of collagen VII. This impairs its assembly into anchoring fibrils that anchor the basement membrane to the underlying dermis.

Diagnostic methods

Diagnosis is based on identification of granular intraepidermal type VII collagen by immunofluorescence mapping and electron-dense stellate bodies on ultrastructural examination. Genetic testing can confirm diagnosis.

Differential diagnosis

The differential diagnosis includes other types of epidermolysis bullosa.

Antenatal diagnosis

Because of the mild course of the disease, antenatal diagnosis is usually not required.

Genetic counseling

Genetic counseling will depend on the mode of inheritance which can be autosomal dominant or recessive.

Management and treatment

Treatment is symptomatic with wound care to prevent secondary infection and reduce scarring.

Prognosis

Overall the prognosis is good.

Last update: May 2021 - Expert reviewer(s): Pr Carmen SALAVASTRU | ERN-Skin*

* European Reference Network

A summary on this disease is available in Français, Logo ERN Español, Logo ERN Deutsch, Logo ERN Italiano, Logo ERN Português, Logo ERN Nederlands Logo ERN Polski
Detailed information

Logo ERN: produced/endorsed by ERN(s) Logo FSMR: produced/endorsed by FSMR(s)

General public
Article for general public
Svenska (2024) - Socialstyrelsen
Guidelines
Emergency guidelines
Français (2012.pdf) - Orphanet Urgences
Anesthesia guidelines
English (2020) - Orphananesthesia
Čeština (2020) - Orphananesthesia
Clinical practice guidelines
English (2020) - Br J Dermatol Logo ERN
English (2020) - Br J Dermatol Logo ERN
English (2019.pdf) - Debra International Logo ERN
English (2016) - Br J Dermatol Logo ERN
English (2014) - Orphanet J Rare Dis Logo ERN
English (2019) - Orphanet J Rare Dis Logo ERN
English (2012) - Int J Paediatr Dent Logo ERN
English (2014) - BMC Med Logo ERN
English (2019.pdf) - Debra International Logo ERN
English (2019) - Orphanet J Rare Dis Logo ERN
English (2020) - Orphanet J Rare Dis Logo ERN
English (2017.pdf) - Wounds International
Español (2017.pdf) - Wounds International
Disease review articles
Clinical genetics review
English (2025) - GeneReviews
Disability
Disability factsheet
Español (2018.pdf) - Orphanet
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