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Adenosine receptors could be promising targets for treating inflammatory skin diseases like psoriasis.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

A scalp infection can look like alopecia areata and get worse if treated incorrectly.

Skin can become dry and thick in hypothyroidism.

Celiac disease requires more than just a gluten-free diet for effective management.

The C3H/HeJ mouse model is useful for studying and testing treatments for alopecia areata.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

GLPLS is a rare skin condition with specific hair loss and skin symptoms.

High proliferative activity and peripheral invasion indicate malignancy in canine sebaceous gland tumors; the term 'epithelioma' should be updated for clarity.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Most skin tumors in the study were benign, with squamous cell carcinoma being the most common malignant type.

A disease causing skin issues in young adult German short-haired pointers is hereditary, with most affected dogs not responding to treatment.

Hair loss in Cronkhite-Canada syndrome may be caused by autoimmune factors, not just stress or malabsorption.

The conclusion is that FFA and LPP have similar scalp biopsy features, making them hard to distinguish histologically, and FFA may be a specific kind of scarring hair loss.

A rare ovarian cancer with a good outlook was found in a woman with unusual hair growth and abdominal symptoms.

Fibrosing alopecia in a pattern distribution is a unique hair loss condition with inflammation and scarring, resembling but distinct from common balding.

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.

A man had a benign pilar cyst on his face, which is rare and was successfully removed by surgery.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Eruptive vellus hair cysts are often missed in diagnoses.

Scalp skin condition LEDS has similar features to Zoon's balanitis, a mucosal skin disorder.

Dermoscopy and trichoscopy are useful for diagnosing skin signs in Dermatomyositis.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

A woman lost her hair from stress after a bee attack and her sister's death.

Lupus can look like hair loss from alopecia areata but needs different treatment.

Alopecia areata can look like frontal fibrosing alopecia, making diagnosis hard.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

A woman with lupus had hair loss and skin issues that were successfully treated with medications.