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The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Cats lose fur due to various reasons, including allergies, infections, genetics, hormones, diet, cancer, stress, and some conditions are treatable while others are not.

Hair growth dysfunction involves various conditions with limited treatment options.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Low-level laser therapy can significantly regrow hair in alopecia areata.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

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

Autoimmune hepatitis in children often affects girls and can be treated successfully with medication.

Eating well and avoiding synthetic hair products are key for healthy hair.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

The study found that certain genes are important for hedgehog skin appendage development and immunity, with spines possibly evolving for protection and infection resistance.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Patients with one autoimmune disease should be checked for other autoimmune disorders.

An 87-year-old woman was diagnosed with type 3 autoimmune polyendocrine syndrome and had multiple autoimmune issues.

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

Older hair follicle stem cells have a reduced ability to renew themselves, leading to more hair loss.

Both Th1 and Th2 immune responses are increased in alopecia areata, with Th2 response more strongly linked to how severe the disease is.

Activating Nrf2 helps wounds heal faster by increasing hair follicle stem cells.

Topical tofacitinib is effective in promoting hair growth for non-scarring alopecia.

Nonshaven follicular unit extraction is a highly satisfactory method for restoring pubic hair.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

The April 2016 JEADV issue covered various dermatology topics, including psoriasis, psoriatic arthritis, mTOR inhibitors, autoimmune diseases, photodynamic therapy, viral DNA in skin diseases, chronic hand eczema, and female hair loss.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

An 8-year-old girl had nail and hair issues that improved without specific treatment, but fungal nail infection was hard to cure.

The conclusion is that understanding how patterns form in biology is crucial for advancing research and medical science.