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Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

The document concludes that oral finasteride and topical minoxidil are effective for genetic hair loss, while other treatments for different types of hair loss show promise but need more research.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

Low-dose radiation affects hair stem cell function and survival by changing their genetic material's structure.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

A woman experienced severe side effects from a drug due to a specific genetic variation, suggesting genetic testing could prevent such risks.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

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.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

Some skin tumors from hair follicles and glands can be linked to genetic syndromes and may be benign or malignant.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Systemic immunotherapies are used for immune-related hair loss but not usually for genetic hair loss, unless the patient has both conditions.

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 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Minoxidil and finasteride are the only FDA-approved treatments for hair loss caused by genetic and hormonal factors, but their effectiveness is often doubted, indicating a need for new treatments.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

A 23-year-old woman's missed periods were caused by a rare genetic disorder treated with hormone patches.

NSG mice had the most mites, and genetic factors affect immune response and susceptibility.

A woman with lupus also developed a severe skin condition linked to a genetic factor.