Graham Little-piccardi-lassueur Syndrome
Graham Little-Piccardi-Lassueur syndrome is a variant of lichen planopilaris (see this term) characterized by the clinical triad of progressive cicatricial (scarring) alopecia of the scalp, follicular keratotic papules on glabrous skin, and variable alopecia of the axillae and groin.
Genes related to Graham Little-piccardi-lassueur Syndrome
Clinical FeaturesPhenotypes and symptoms related to Graham Little-piccardi-lassueur Syndrome
- Sparse scalp hair
- Sparse axillary hair
- Sparse pubic hair
- Scarring alopecia of scalp
- Perifollicular hyperkeratosis
Incidence and onset information— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.
Graham Little-piccardi-lassueur Syndrome Is also known as graham little syndrome, piccardi-lassueur-little syndrome.
Researches and researchersCurrently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.
Graham Little-piccardi-lassueur Syndrome Recommended genes panels
|Panel Name, Specifity and genes Tested/covered|
By Fulgent Genetics Fulgent Genetics (United States).
Tempus xT assay.
By Tempus Labs, Inc. (United States).
BCL6, RIT1, BCL7A, BCR, ROS1, RPL5, RPS15, RPS6KB1, RUNX1, RXRA, BLM, SDHA, SDHB, SDHC, SDHD, SEC23B, SEMA3C, BMPR1A, SF3B1, SRSF2 , (...)
View the complete list with 555 more genes
You can get up to -6 more panels with our dedicated toolLearn more
Sources and references
You can check the following sources for additional information.ORPHANET Rare Disease Search Engine
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