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Adding Triamcinolone to the anesthetic can reduce swelling after hair transplants, and using Platelet-Rich Plasma can improve hair thickness and patient satisfaction. The SRD5A2 gene also plays a key role in the success of hair transplants.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

A baby with KID syndrome died from infections and organ failure at 18 months old.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

Prunus mira Koehne is valuable for hair growth and has potential for sustainable use, but needs more research and conservation.

Wire brush snares are best for collecting Eurasian Lynx hair for DNA analysis.

Some women with PCOS have rare genetic variants linked to the condition.

Genetic factors could lead to personalized treatments for hair loss.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

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.

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

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

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

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

The C3H/HeJ mouse model is useful for studying and testing treatments for alopecia areata.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

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