Search

everythinglearnresearchcommunity

for

Search:↓

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

The 2024 guideline updates recommendations for genetic testing, imaging, and sperm retrieval in male infertility.

Finasteride may negatively affect male fertility.

Certain gene variations are not a major cause of male infertility in Nigerian men.

A thorough initial check-up is essential before sperm banking to ensure the best chance of preserving good quality sperm.

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.

Products should be called 'sperm-safe' only after thorough, well-designed tests.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

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

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

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

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

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

Finasteride may cause sexual side effects like erectile dysfunction, but they are reversible and affect less than 2% of men.

The skin and thymus develop similarly to protect and support immunity.

DA-9401 helps protect rat testis from finasteride damage.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

Hair changes can indicate systemic diseases or medication effects.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

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.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.