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Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

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

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

The document concludes that managing Dunnigan-Type Familial Partial Lipodystrophy involves treating associated health issues and using medications like metformin and leptin replacement.

Hair usually grows back 1-3 months after treatment for anagen effluvium, and children with Loose Anagen Hair Syndrome often improve by adolescence.

Too much androgen can cause hair loss; finasteride may help.

Finasteride caused blisters on hands and feet.

Hair loss is caused by genetics and hormones, diagnosed through examination and biopsy, and treated with medications or surgery.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

The woman's rare combination of diseases suggests an unknown factor may predispose individuals to multiple endocrine diseases.

Looking at skin can help find and treat serious diseases early.

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

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Treatment with plasma rich in growth factors improved hair density and thickness for hair loss patients.

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.

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.

Minoxidil 2% effectively treats female hair loss, promoting growth and density.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Male pattern baldness involves hormone-related hair thinning, shorter hair, and inflammation.

Researchers found a gene mutation responsible for a rare hair loss condition.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Recent hair loss research shows some progress, especially in understanding male pattern baldness, but effective treatments for many types of hair loss are still lacking.