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Finasteride, when given in high oral doses to pregnant monkeys, caused genital abnormalities in male fetuses, but not in female fetuses or those exposed to intravenous finasteride.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

Blocking the enzyme 5α-reductase can shrink the prostate and help treat enlarged prostate issues.

Exposure to finasteride in the womb caused lasting reproductive issues in male rats.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Some skin diseases and their treatments can negatively affect male fertility.

People in Jeddah know about Vitamin D and its sources but are unclear on how much they need daily, and while many women take supplements, attitudes towards increasing Vitamin D levels vary.

A rare benign skin nodule was found on the buttock, a unique location for this condition.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Hormones, especially testosterone and DHT, are key for penis development and function, and testosterone therapy may help with erectile dysfunction in those with low levels.

There are various effective hormone treatments for puberty induction in boys and girls with hypogonadism, and starting treatment early is important.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

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

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

The type 3 IP3 receptor is important for controlling hair loss and growth.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Giving dihydrotachysterol to mother rats caused skin hardening and bone issues in their babies through milk.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

Scalp biopsies are important for diagnosing hair loss conditions.

The Li-Pa/Ca and Do/Ca chemotherapy regimens for serous ovarian cancer showed better short-term and long-term results than the Pa/Ca regimen.

Young dogs in Odisha with dermatitis are most often infected by Microsporum fungus, and Miconazole is the most effective treatment.

Men are increasingly interested in cosmetic treatments that enhance masculinity and address aging without downtime, with tailored approaches for different ethnicities and a focus on hair restoration and body contouring.

A new mouse mutation causes skin and hair defects due to a gene change.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

ULBP3 levels are higher in Tinea capitis patients and may help predict the disease's severity.

Chemotherapy causes hair loss by damaging hair follicles and stem cells, with more research needed for prevention and treatment.