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Folliculitis Decalvans and Frontal Fibrosing Alopecia can coexist in people with darker skin, showing features of both conditions.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

The most common form of PCOS in the group was anovulatory PCOS, with no cases of obese PCOS, highlighting the importance of assessing lean women with menstrual issues.

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

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.

The article concludes that global standardization in PCOS research is crucial for accurate diagnosis and understanding of the condition.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

DNA markers can predict physical traits for forensic use, but there are ethical and technical challenges.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

A specific gene mutation causes congenital hair loss.

Biotinidase deficiency has various symptoms and can be treated with biotin supplements.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Understanding phenotypic plasticity is crucial for developing effective cancer therapies.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Patients with both connective tissue disease and acid reflux are more likely to have certain symptoms and physical signs.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Women with PCOS often have hair loss, which is linked to acne or excess body hair but not to worse hormone or metabolic issues.

Both classical and L-type atypical BSE from cattle can infect goats with different incubation times, and tests can distinguish between the two strains.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

PCOS is a hormonal disorder causing symptoms like excess hair, acne, irregular periods, and fertility issues.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

T-cells in alopecia areata scalp show abnormal regulation, leading to less inflammation.

Growth media with sucrose and gelrite significantly enhance Arabidopsis root hair growth.