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Sensitive scalp causes discomfort and may relate to hair loss, with treatment focusing on scalp care and medication.

Hair grew in a man's mouth due to a rare condition called heterotopia.

Trichoscopy can reliably distinguish between alopecia areata and trichotillomania.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Trichilemmal carcinoma shares genetic changes with other skin cancers, suggesting similar causes and potential treatments.

Trichilemmal cysts may form from hair follicle outer root sheath growth.

Many people with hair loss experience scalp pain known as trichodynia, but the causes are unclear and treatments vary.

Escitalopram helped a woman with hair-pulling due to long COVID.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Giant solitary trichoepithelioma is a rare, usually non-cancerous hair follicle tumor that can sometimes turn into skin cancer.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Increased hair growth after a cast is temporary and harmless.

Monilethrix causes different levels of hair loss in family members.

Hair-thread tourniquet syndrome needs more awareness and discussion in dermatology.

Plica polonica is a rare condition where hair becomes irreversibly tangled, and the treatment is to cut the matted hair.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Removing hair wrapped around the labia quickly prevents serious tissue damage.

Trichotillomania treatment is most successful with a mix of behavioral therapy, medication, and social support.

A specific gene mutation causes Olmsted syndrome.

Bupropion SR may help treat trichotillomania.

Most children with pediatric trachyonychia improve over time, regardless of treatment.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Tricholemmoma is linked to Cowden syndrome and can be benign or malignant.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

Tigason improved hair growth in a boy with monilethrix without side effects.

Hair-thread Tourniquet Syndrome, where hair or thread tightly wraps around a body part, is not rare and requires early detection to prevent serious damage.

Early detection and removal of hair can prevent damage in hair-thread tourniquet syndrome.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Hair-tourniquet syndrome can cause serious toe injuries in infants but can be treated if found early.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.