Galli–Galli disease
| Galli–Galli disease | |
|---|---|
| Specialty | Dermatology |
Galli–Galli disease is a rare inherited condition that has close resemblance clinically to
skin lesions that are 1- to 2-mm slightly keratotic red to dark brown papules which are focally confluent in a reticulate pattern.[1]: 856 The disease is also characterized by slowly progressive and disfiguring reticulate hyperpigmentation of the flexures, clinically and histopathologically diagnostic for Dowling-Degos disease but also associated with suprabasal, nondyskeratotic acantholysis.[2][3]
See also
- List of cutaneous conditions
- Skin lesion
References
- ISBN 0-7216-2921-0.
- ^ Journal of the American Academy of Dermatology ISSN 0190-9622 CODEN JAADDB
- ISBN 978-1-4160-2999-1.
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