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Male pattern baldness involves hormone-related hair thinning, shorter hair, and inflammation.

Hair loss in Cronkhite-Canada syndrome is reversible by treating the gut issues and doesn't need steroid treatment for the hair itself.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Researchers found a gene mutation responsible for a rare hair loss condition.

Children with short anagen syndrome usually see their hair condition improve as they get older.

Loose Anagen Syndrome is more common in females and may be inherited, often confused with other hair disorders, and lacks evidence for biotin treatment effectiveness.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Different combinations of human hair keratins affect how hair fibers form.

A 72-year-old man had severe fatigue, weight loss, and frequent loose stools.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.

Hair restoration surgery can effectively increase pubic hair density, with patient satisfaction and natural results largely depending on the chosen hair pattern and graft design.

Skin problems can be signs of hormone-related disorders and recognizing them early is important for treatment.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

Successful eyebrow restoration can be done using careful hair transplant techniques and choosing the right patients.

Hair changes can indicate systemic diseases or medication effects.

ILK and ELMO2 help cells move and stick together, important for wound healing and hair growth.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

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

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

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.

Cells from certain embryo parts can induce head formation in another embryo, involving complex signaling pathways.

Mutation in hairless gene may increase hair loss risk.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Hair loss in children is diagnosed and treated differently than in adults, with different common causes and a focus on less invasive methods.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.