Search

everythinglearnresearchcommunity

for

Search:↓

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.

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.

A baby boy had two types of temporary hair loss at birth, which might be two forms of newborn hair loss combined.

Assessing newborn scalp hair can reveal important health information.

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.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

Trichoscopy is good for telling apart tinea capitis and alopecia areata in kids.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

A baby had a rare case of widespread milia, which was treated and is being monitored.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Neurohormones help control skin health and could treat skin disorders.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.