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Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

The gene Prss53 affects hair shape and bone development in rabbits.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

The study found that the protein Dkk4 helps regulate hair growth by controlling Wnt signaling in mice.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

Embryonic and adult stem cells are valuable for improving skin grafts and cell therapy.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

A20 protein is crucial for normal skin and hair development.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

Edar signaling is crucial for proper hair follicle development and function.

Red and infrared light therapy improves hair growth in balding patients.

A 73-year-old man's grey-white hair turned dark brown after eczema treatment.

Lactic acid cream can help improve skin bumps known as eruptive vellus hair cysts.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

The document concludes that non-endocrine alopecia in pets varies in treatment effectiveness and often has a poor prognosis, especially in cats.

Congenital atrichia is a rare condition where children are born without hair, and treatment is often ineffective.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.