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Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Oral retinoids are effective for various skin conditions but have side effects and should not be used during pregnancy.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

The most common skin problems in Indian children are infections and eczemas.

The study concluded that key signs of Keratosis follicularis spinulosa decalvans are changes in terminal hair and vellus hair follicles, which likely start the inflammation and damage to hair follicles.

Long-term use of Risperidone may be linked to a serious skin condition in bipolar patients, affecting their overall well-being.

Iron deficiency might contribute to hair loss in women.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

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

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

A 23-year-old woman's missed periods were caused by a rare genetic disorder treated with hormone patches.

Androgenic steroids can slow down or stop the growth of certain skin fungi.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Tissue environment greatly affects the unique epigenetic makeup of regulatory T cells, which could impact autoimmune disease treatment.

Creating stronger blockers for skin enzymes might lead to better treatment for conditions like acne and excessive hair growth.

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

Surgery on a baby with a skin disorder improved eyelid position and eye health.

EGF and FGF help hair growth by affecting cell differentiation and fiber growth.

The document concludes that understanding hair follicle histology and the hair cycle is crucial for diagnosing alopecia.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

Systemic diseases can cause hair loss, which is often reversible with treatment.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Some diseases can improve the outcomes of other diseases, leading to new treatment possibilities.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Glucocorticoids for progressive muscular dystrophy in children don't improve muscle strength or function but do increase certain side effects.

Removing centrosomes from skin cells leads to thinner skin and stops hair growth, but does not greatly affect skin cell differentiation.