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Chromosomal differences affect how muscle cells respond to testosterone.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

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.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

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.

Passiflora incarnata may help with anxiety but has risks and drug interactions. There's a genetic link between Fragile X Syndrome and Autism Spectrum Disorder. 6.7% of urine cultures showed hospital-acquired urinary tract infections. Children used screens more during COVID-19, causing various health complaints. Autism Spectrum Disorder is often underdiagnosed in females. Dissociative disorders in childhood sexual abuse victims are more common in males. Most pregnant teenagers are not dissatisfied with their body image but worry about weight. Diagnosing tuberculosis after knee surgery is challenging due to non-specific symptoms. Post-COVID-19 syndrome is more common in older, severely affected patients. Psychiatrists should be part of pain management teams due to the psychological aspects of pain.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

A 7-month-old girl with a rare skin disorder died because diagnosis was delayed.

Researchers found a genetic region that influences the number of coat layers in dogs.

Certain genes are linked to the risk of developing Alopecia Areata.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

The document concludes that current treatments for androgenic alopecia are not fully effective, but new therapies like botulinum toxin and PRP show promise, and future gene therapy could be beneficial.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

Genes and hormones cause hair loss, with four genes contributing equally.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Certain gene variations might be linked to severe acne in women but not in men.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

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

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.