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A multidisciplinary approach with virtual sessions effectively reduces compulsive hair pulling in young people.

Early intervention and continuous treatment are key for managing hereditary hair loss effectively.

Uncombable hair syndrome causes dry, frizzy hair that can't be combed flat, seen in a young child.

Skin changes can help identify eating disorders early.

Trichoscopy is useful for diagnosing Netherton syndrome in children with skin issues.

Systemic diseases can cause hair loss, which is often reversible with treatment.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

A 10-year-old boy had the earliest reported case of hair that became progressively kinkier but eventually returned to normal on its own.

Disruptions in sleep-wake cycles can cause health problems like mental, metabolic, and heart diseases, and cancer.

Alopecia linked to higher anxiety and personality disorders.

Autoimmune diseases can change hair texture, but treatment can restore it.

PRP patients show varied symptoms and need more research to understand related conditions.

Alopecia areata is an autoimmune hair loss condition linked to genetic factors.

Dengue fever can cause hair loss that may lead to serious psychological issues like Body Dysmorphic Disorder in young women.

MicroRNAs and AI can improve cashmere goat hair quality and aid in hair disorder diagnosis.

Next-generation sequencing greatly improves understanding and treatment of genetic hair disorders.

Plica Polonica is a rare hair disorder causing severe matting, managed by detangling or cutting, and prevented with regular hair care.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Diagnose and manage CCCA with thorough history, exams, and labs; treat with anti-inflammatory agents, stress reduction, and stopping harmful hair practices.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

Children with darker skin tones can have specific skin conditions that need tailored treatments.

Hormonal changes after childbirth and menopause can lead to women's hair loss and facial hair growth, with a need for better treatments.

The diagnosis of polycystic ovary syndrome (PCOS) requires a detailed patient history, ultrasound scanning, hormone level checks, and assessments of ovulation, obesity, and insulin resistance. It's a variable condition that needs individualized management and is a significant risk factor for type 2 diabetes.

Trichotillomania is often misdiagnosed as alopecia areata and can be treated effectively with N-acetylcysteine and psychotropic drugs.

Personalized medicine is important for treating skin disorders, with new treatments and connections to hormones and genetics being explored.

Six genetic conditions are often linked to complete scalp hair loss in children.

Uncombable hair syndrome is linked to Zellweger syndrome.

New non-invasive techniques can improve diagnosis and treatment of scalp and hair diseases.

Identifying and treating deficiencies and conditions can stop or reverse premature greying in children.

Identifying and treating deficiencies and conditions can stop or reverse premature greying in children.