genodermatosis
Sign in to saveAlso known as genetic skin disease, Genetic Skin Diseases, Skin Disease, Genetic, Disease, Genetic Skin, Diseases, Genetic Skin, genetic skin disorder, Skin Diseases, Genetic
Genodermatosis is a hereditary skin disease with three inherited modes including single gene inheritance, multiple gene inheritance and chromosome inheritance. There are many different types of genodermatosis; the prevalence of genodermatosis ranges from 1 per 6000 people to 1 per 500,000 people. Genodermatosis has influence on the texture, color and structure of skin cuticle and connective tissue. Specific lesion site and clinical manifestations on the body vary depending on the type. In spite of the variety and complexity of genodermatosis, there are still some common methods that can help p
Research
97,603 papers- Incontinentia pigmenti: multisistemic genodermatosis.Boletin medico del Hospital Infantil de Mexico · 2020
- A current and online genodermatosis database.The British journal of dermatology · 2007
- Classic Dowling Degos disease: a rare genodermatosis.Italian journal of dermatology and venereology · 2021
- Érythème annulaire centrifuge chez un enfant.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2023
- VEXAS syndrome and immune-mediated rheumatic diseases: overlaps in clinical features and mechanisms.The Lancet. Rheumatology · 2025
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Article
32 sectionsContents
- Hereditary modes
- Single gene (monogenic)
- Autosomal dominant inheritance
- Autosomal recessive inheritance
- X-linked dominant inheritance
- X-linked recessive inheritance
- Multiple gene (polygenic)
- Chromosome
- Types
- Common types
- Ichthyosis
- Rare types
- Michelin tyre baby syndrome
- Epidermolysis bullosa
- Pachyonychia congenita
- Epidermolytic palmoplantar keratoderma
- Hereditary benign intraepithelial dyskeratosis
- Epidermolytic hyperkeratosis
- Hidrotic ectodermal dysplasia
- Diagnostic methods
- Therapy
- Prevention and care
- Ichthyosis
- Epidermolysis bullosa
- Epidermolytic hyperkeratosis
- Pachyonychia congenita
- [[Neurofibromatosis type I]]
- Therapeutic methods
- Effects
- See also
- References
- External links
Genodermatosis is a hereditary skin disease with three inherited modes including single gene inheritance, multiple gene inheritance and chromosome inheritance. There are many different types of genodermatosis; the prevalence of genodermatosis ranges from 1 per 6000 people to 1 per 500,000 people. Genodermatosis has influence on the texture, color and structure of skin cuticle and connective tissue. Specific lesion site and clinical manifestations on the body vary depending on the type. In spite of the variety and complexity of genodermatosis, there are still some common methods that can help people diagnose. After diagnosis, different types of genodermatosis require different levels of therapy including interventions, nursing interventions and treatments. Among that, research of therapy for some new, complex and rare types are still in the developing stage. The impact of genodermatosis not only can be seen in the body but also can be seen in all aspects of patients' life, including but not limited to psychological, family life, economic conditions and social activities. Accordingly, the patients need treatment, support and help in these areas.
== Hereditary modes == Genodermatosis is inherited in three modes: single gene inheritance, multiple gene inheritance and chromosome inheritance.