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Deferasirox effectively reduces iron overload in ß-thalassemia patients but may cause some manageable side effects.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

The document concludes that the girl's hairlessness is likely inherited from her parents.

Certain genetic variations in IL-16 may increase the risk of 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.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

Prolactin levels and gene polymorphism are not linked to vitiligo severity but are related to BMI.

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

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Different scalp and hair disorders are more common in certain ethnic groups, with the most common being androgenetic alopecia, which is treated with medications like minoxidil and finasteride.

Stem cells regenerate tissues and their behavior varies by environment, suggesting the hematopoietic system model may need revision.

Female hair loss is often hereditary and can be treated with medication, hair transplants, and lasers.

Androgens like testosterone affect skin health and can lead to conditions such as acne and hair loss, with various treatments available.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

Maintaining DNA integrity in stem cells is crucial to prevent aging and cancer.

Early skin biopsy helps diagnose and manage severe skin conditions in babies.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Understanding skin patterns can help us learn about skin diseases and their treatments.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

The essay suggests hair loss might be caused by changes in skull bones.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

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

People with Down's syndrome are more likely to have syringomas.