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Mast cells play a significant role in hair loss conditions like male pattern hair loss and alopecia areata.

The conclusion is that accurate diagnosis of different types of hair loss requires good teamwork between skin doctors and lab experts.

Pediatricians should treat some hair loss types in children and refer others to a dermatologist.

Four genes are potential markers for hair loss condition alopecia areata, linked to a specific type of cell death.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Finasteride, often used for hair loss, can potentially cause cataracts.

Dermal Wnt/β-catenin signaling is important for the proper size and development of hair follicles.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Loose Anagen Syndrome is a hair condition where hairs can be easily pulled out, mainly affecting young girls, and may improve on its own or with treatment.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Hair usually grows back 1-3 months after treatment for anagen effluvium, and children with Loose Anagen Hair Syndrome often improve by adolescence.

Black dots under trichoscopy can appear in different hair and scalp conditions, not just in alopecia areata.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

Cell death shapes skin stem cell environments, affecting inflammation, repair, and cancer.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Non-invasive methods can effectively diagnose and manage alopecia areata.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

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.

Acne vulgaris is a common skin condition that can cause low self-esteem and depression, and early treatment is important to prevent scarring.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

A man developed autoimmune issues after a transplant, improved with treatment, but died from leukemia relapse.

Public interest in skin issues changed during COVID-19, with more focus on dry skin, hair problems, and hand eczema.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.