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Family-based treatment is the best outpatient care for stable teens with anorexia, and more research is needed on medication and treatment effectiveness for young people with eating disorders.

Detailed history and physical examination are crucial for diagnosing hair loss.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Most hair loss can be diagnosed with patient history and physical exam, and a few common types make up most cases.

Guidelines for diagnosing common hair loss include detailed history, clinical examination, and various diagnostic techniques.

Evaluate postmenopausal women with high androgen levels using medical history, physical exams, lab tests, and imaging to manage health risks.

Excessive hair growth can be assessed by history, exam, and blood tests, and treated with medication like dexamethasone, birth control pills, and spironolactone.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Doctors should use a detailed patient history and physical exam to diagnose joint pain, and consult a rheumatologist early for suspected autoimmune diseases.

Obstetrician/gynecologists can diagnose and manage female hair loss with careful history taking and examination.

The document concludes that accurate diagnosis of alopecia in children relies on thorough examination and history, and while treatments exist, none can alter the course of alopecia areata, which can significantly affect a child's psychological well-being.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

Women with PCOS may take longer to get pregnant but can have a normal family size, and should manage their overall health to reduce long-term health risks.

Finasteride can cause serious emotional side effects; doctors should check patients' mental health history before prescribing.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

Some African American women experience central scalp hair loss, often linked to a history of fungal scalp infection.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

The document concludes that hirsutism is the main sign for diagnosing hyperandrogenism, which requires a detailed patient history and physical exam.

The conclusion is that obesity should be managed with a slow, balanced approach to diet and exercise, with medication and surgery as additional options, and education and access to care are important.

Hair loss in women is often due to hereditary conditions or stress, and while treatments like minoxidil can help, diagnosis and management require medical guidance.

Despite progress, better treatments and understanding are needed for the high rates of long-term issues and deaths linked to eating disorders.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

Children's hair loss has many causes and requires careful diagnosis and personalized treatment, including emotional support.

Taiwan reported its first case of a rare scalp condition with no clear cause or treatment.

People in Jeddah know about Vitamin D and its sources but are unclear on how much they need daily, and while many women take supplements, attitudes towards increasing Vitamin D levels vary.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.