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Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Adrenal gland disease is common in ferrets and causes hair loss and other symptoms.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Boxer dogs may have a genetic skin condition that worsens seasonally and can be treated with certain medications.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

Male pattern baldness is often genetic and linked to a hormone, with treatments like finasteride and minoxidil being effective for some men.

Erosive pustular dermatosis of the scalp is a rare condition that causes scarring hair loss, mainly in older women, and requires ongoing treatment.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

The investigation found no work-related causes for employee hair loss at Equifax Payment Services, and the environment was not hazardous.

The document says a skin condition called alopecia areata causes hair loss and stress, and is treated with strong skin creams, injections, or other therapies, but treatment success varies.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

Acute telogen effluvium can be resolved by addressing causes, but chronic telogen effluvium is harder to treat.

Chitosan slows root hair growth and causes a buildup of callose at low concentrations, but at high concentrations, it only inhibits growth without callose buildup.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Removing Lrig1-positive stem cells in mice causes temporary loss of sebaceous glands.

The document concludes that scalp conditions have various causes and can present in many different ways.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

The meeting covered advances in understanding hair growth, causes of hair loss, and potential treatments.

Cyclooxygenase-2 overexpression in mice skin causes hair loss like human androgenetic alopecia.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

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

The conclusion is that future hair loss treatments should target the root causes of hair thinning, not just promote hair growth.