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Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Amenorrhea, or the absence of periods, should be evaluated by age 15 or within five years of early breast development, and is most commonly caused by conditions like polycystic ovary syndrome and hypothalamic amenorrhea.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Men are more likely to have severe respiratory viral infections like COVID-19 due to hormonal and genetic differences, while women generally have stronger immune responses.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

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

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

Down Syndrome patients with Alopecia Areata often have hypothyroidism and specific immune abnormalities.

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

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

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.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

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.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The study found that heart disease is common in people with PCOS and that being overweight is a major risk factor; lifestyle changes and medication are important for management.

Understanding how acne develops in different diseases could lead to new treatments.

Different processes create patterns in skin and things like hair and feathers.

Natural gene therapy shows promise for treating skin disorders like epidermolysis bullosa.

Understanding skin patterns can help us learn about skin diseases and their treatments.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Estrogen and prolactin may play bigger roles in female hair loss than previously thought.