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Growth hormone levels affect hair growth and loss, with too much causing excess hair and too little leading to hair loss.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

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

Loose Anagen Syndrome is a hair condition where hairs can be easily pulled out, mainly affecting young girls, and may improve on its own or with treatment.

Loose Anagen Syndrome is more common in females and may be inherited, often confused with other hair disorders, and lacks evidence for biotin treatment effectiveness.

Loose anagen hair syndrome, often affecting young girls, can be diagnosed with a hair-pull test and usually gets better on its own, but severe cases may need treatment.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Some skin diseases and their treatments can negatively affect male fertility.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

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

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

Keratosis pilaris is a common skin condition causing a bumpy texture, sometimes linked to other diseases, with various treatments available.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

The document is a detailed medical reference on skin and genetic disorders.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

COVID-19 may harm male fertility and damage the reproductive system.