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A child with rough nails also had hair loss and allergies.

A new genetic mutation was found causing hair and eye issues in a boy.

CRPS type I is a complex pain condition with no proven cure, requiring personalized treatment.

A 12-year-old boy with twenty nail dystrophy, a condition affecting all nails, was treated conservatively due to its self-limiting nature and good prognosis.

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

Annurca apple extract may protect mouse hair from damage by chemotherapy and could help treat hair loss without promoting cancer growth.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

LncRNAs play a crucial role in muscle regulation and could help develop treatments for Duchenne muscular dystrophy.

Transplanting a person's own hair can heal chronic wounds in certain skin conditions.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

Targeting specific T cells may help treat alopecia areata.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

Treatment improved some symptoms but not all.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Chemotherapy affects blood vessels in hair follicles, not stem cells, allowing hair regrowth.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Cyclosporine A slows down hair loss from chemotherapy in mice, while dexamethasone increases hair loss but speeds up regrowth.

Epidermolysis bullosa is a genetic disease causing fragile skin and blisters in both animals and humans.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Diagnosing hair loss disorders needs clinical, dermoscopic, and histological differences, and checking menstrual cycle, weight changes, drug therapy, and nail changes.

PTH-CBD could help prevent and treat hair loss caused by chemotherapy in mice.

Alopecia Areata Incognita causes widespread hair thinning, and treatment with systemic corticosteroids and psychiatric support can lead to remission.

The paper suggests that telogen effluvium, a type of hair loss, may be a long-lasting condition triggered by stress or illness in people whose hair growth is unusually synchronized.

The author clarified that Alopecia Areata Incognita (AAI) and diffuse Alopecia Areata (AA) are different conditions and the case discussed was actually AA, not AAI.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

The author clarifies that alopecia areata incognito and diffuse alopecia areata are different types of hair loss with unique symptoms and challenges in diagnosis.

SLE patients experience hair loss similar to telogen effluvium, with hair damage and immune activity at hair follicles.

Contaminated wheat caused hair loss and other symptoms due to high selenium, but washing it with alkaline water helped.