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Type 2 diabetes, bacterial scalp infections, and tight hairstyles like braids and weaves are linked to a higher risk of a scarring hair loss condition in African American women.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Male pattern baldness involves genetics, hormones, and needs better treatments.

Genes and hormones cause hair loss, with four genes contributing equally.

Men with a family history of hair loss are more likely to experience it themselves, especially if both parents have hair loss.

Longer hair loss leads to more severe CCCA; early treatment and avoiding damaging hairstyles help regrowth.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

An 18-year-old girl with pemphigus vulgaris needed strong medication and careful treatment due to ineffective initial therapies and side effects.

AGA is a common hair loss affecting both genders, treated with various therapies to promote regrowth and slow thinning.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

Hair loss needs more research for better treatments.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

Smoking linked to hair loss in Asian men.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Small white dots on the scalp seen with a dermoscope correspond to sweat ducts and vary with different hair disorders.

Alopecia common in teens, may indicate endocrine issue, minoxidil effective treatment.

CCCA is a common scarring hair loss in African descent women, possibly linked to genetics, hair care practices, and health issues like diabetes.

Children with autoimmune gastritis showed improved intestinal health over time and should be checked for other autoimmune conditions.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

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

A new gene mutation causes insulin resistance in a girl and her mother.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

Alopecia areata often starts around age 23, can be permanent in 30% of cases, and treatments are usually temporary.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

The article discusses debates on hair transplant techniques, safe donor areas, PRP use, and practitioner qualifications in hair restoration.

Many women with hair loss also have thyroid issues, high blood pressure, and low Vitamin D.