Trichotillomania; Ttm
Description
Trichotillomania (TTM) is a neuropsychiatric disorder characterized by chronic, repetitive, or compulsive hair pulling resulting in noticeable hair loss. The activity causes distress to the individual and often interferes with functioning. Affected individuals may develop physical complications and often have overlapping psychologic disorders, such as Tourette syndrome (GTS ) or obsessive-compulsive disorder (OCD ) (review by Novak et al., 2009).
Clinical Features
Phenotypes and symptoms related to Trichotillomania; Ttm
- Depressivity
- Alopecia
- Obsessive-compulsive behavior
- Alopecia of scalp
- Hair-pulling
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.
Researches and researchers
Currently, 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.Trichotillomania; Ttm Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
SLITRK1. Complete sequencing.
By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).
SLITRK1
Specificity
100 %
Genes
100 % |
Tourette syndrome (sequence analysis of SLITRK1 gene).
By CGC Genetics (Portugal).
SLITRK1
Specificity
100 %
Genes
100 % |
Tourette syndrome.
By Centogene AG - the Rare Disease Company (Germany).
SLITRK1
Specificity
100 %
Genes
100 % |
Gilles de la Tourette Syndrom.
By Praxis fuer Humangenetik Wien (Austria).
SLITRK1
Specificity
100 %
Genes
100 % |
Trichotillomania.
By Praxis fuer Humangenetik Wien (Austria).
SLITRK1
Specificity
100 %
Genes
100 % |
Gilles de la Tourette Syndrom.
By MedGene (Slovakia).
SLITRK1
Specificity
100 %
Genes
100 % |
Trichotillomania.
By MedGene (Slovakia).
SLITRK1
Specificity
100 %
Genes
100 % |
SLITRK1.
By Fulgent Genetics Fulgent Genetics (United States).
SLITRK1
Specificity
100 %
Genes
100 % |
You can get up to 3 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
MESH OMIM Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like NEPHROTIC SYNDROME, TYPE 11; NPHS11 FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3 LEUKOTRIENE C4 SYNTHASE DEFICIENCY KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA; KLICK 8P11.2 DELETION SYNDROME EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2; EBSB2 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC