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The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Hair is a complex organ, and understanding its detailed structure and growth phases is crucial for analyzing substances within it.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Use trichoscopy to diagnose hair loss; treat with minoxidil, finasteride, or dutasteride; consider platelet-rich plasma and spironolactone.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Hair health is influenced by genetics, aging, and environmental factors, with proper care needed to maintain it.

Gene mutations can cause problems in male genital development.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.

Men born very underweight had higher estrogen levels but normal reproduction compared to normal birth weight men.

A form of vitamin E promotes hair growth by activating a specific skin pathway.

Gonadal hormones may influence sex differences in play fighting in animals, but their effect on human spatial behavior is unclear and needs more research.

EGF controls hair growth by regulating hair follicles' growth phases.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Pregnancy can cause skin changes like pigmentation, stretch marks, and temporary hair loss, which often worry the expectant individual.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

IRS-specific genes in Tan sheep hair follicles peak at birth and may affect wool crimp.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Treating classic 21-hydroxylase deficiency requires precise glucocorticoid dosing and attention to individual patient needs, with new treatments showing promise.

ICAM-1 helps regulate hair growth cycles and skin remodeling.