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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.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

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.

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.

Trichoblastomas in rabbits are linked to uncontrolled embryonic hair growth and have distinct histological features.

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.

Mutation in hairless gene may increase hair loss risk.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

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.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

PGA-4HGF may help treat hair loss by activating hair growth pathways and extending the hair growth phase.

Key genes can rewire networks, changing skin appendage types.

Bimatoprost 0.03% solution effectively promotes eyebrow growth.

A herbal extract may help treat certain types of hair loss by reducing a specific gene's activity.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

No genetic link between prostaglandins and hair loss found.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.