Search

everythinglearnresearchcommunity

for

Search:↓

Congenital alopecia areata may have genetic links and topical corticosteroids are an effective treatment.

The case suggests that dissecting cellulitis of the scalp can occur in a White child and should be considered when diagnosing pediatric scarring alopecia.

Many people experienced hair loss after having COVID-19, with the worst cases in hospitalized patients, and some saw hair regrowth within six months.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

The conclusion is that different treatments improved hair growth in dogs with Alopecia X, but results varied and not all dogs had complete hair regrowth.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

Stem cell serum effectively treated hair loss caused by COVID-19.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Dissecting cellulitis of the scalp is a condition that causes inflammation and scarring on the scalp, mainly affecting African-American men, and can lead to permanent hair loss.

A woman's hair loss was initially misdiagnosed as scarring hair loss but was actually a treatable autoimmune hair loss.

Tofacitinib improved arthritis and partially improved hair loss in a lupus patient without side effects.

A young man with an unusual type of scarring hair loss suggests a possible new variant of a known scalp condition.

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

EMT helps heal tissues but can cause scarring and other issues if prolonged.

The study found that alopecia areata is strongly linked to autoimmune diseases and may indicate a genetic predisposition to such conditions.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

Ovol2 is important for proper skin healing and hair growth.

Imipramine and pseudoephedrine treatment can effectively restore normal ejaculation in patients with diabetes, increasing their chances for pregnancy.

PRP is an effective and safe treatment for alopecia areata.

An 8-year-old boy with hair loss had hair regrowth and responded well to clobetasol propionate treatment.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

The study found that severe alopecia areata affects any age, treatments often give temporary results, and some factors predict worse outcomes.

People with certain allergic conditions or higher white blood cell counts have more severe hair loss, and treating hair and nail side effects early in melanoma therapy can improve quality of life.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Early attempts at using cloned cells for hair transplants failed, but 3D cell growth showed some promise.

Frontal fibrosing alopecia causes hairline recession and eyebrow loss in postmenopausal women.

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