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The study concluded that similar pathways regulate hair growth in dogs and mice, and these pathways are disrupted in dogs with Alopecia X, affecting stem cells and hormone metabolism.

A girl with Netherton syndrome was able to eat wheat without allergies after a special treatment.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

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.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Improving maternal diets can prevent severe health issues, including death, from goiter in goat kids.

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.

Trichoepitheliomas can be hard to distinguish from other skin conditions and often start in teenage years.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

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.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A 9-year-old Hispanic girl has Uncombable Hair Syndrome, which may improve with age and biotin treatment.

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

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.

Minoxidil, applied on the skin or taken orally, can improve hair growth in kids, but more research is needed due to possible side effects.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Scrotal rejuvenation treats aging-related changes in men's scrotum using methods like medication, hair transplantation, and surgery.

Regulatory γδ T cells help protect hair follicles from alopecia areata and promote hair regrowth.

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.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.