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Hair examination helps diagnose rare neurological diseases in children.

A young girl's foot lesion was actually a rare condition caused by a hair fragment under the skin, not a parasite.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

Telogen effluvium is a condition that causes temporary hair loss due to stress or shock to the body.

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

A 13-year-old boy had a rare, stable type of hair loss with little chance of regrowth, but treatment is available for looks.

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.

Telogen effluvium is a condition that causes temporary hair loss.

Valproic acid may cause temporary hair changes like loss or thinning in children.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

The document did not provide specific information on Telogen Effluvium.

Swimming in Lake Malawi can lead to schistosomiasis, hepatitis B vaccine might cause temporary hair loss, and certain drinks affect kidney stone risk.

Children's skin diseases need special care and treatment.

Skin diseases in Turkish children vary by age and gender, with infections, eczema, acne, and allergies most common.

A preterm baby's toes were saved from damage by quickly removing a thread that was cutting off circulation.

The document discusses a young boy with autism and early puberty but does not provide a conclusion on managing his behavior.

Polycystic ovary syndrome is a common hormonal disorder in women that affects health and fertility.

Neonatal lupus symptoms usually resolve, but some children may develop other autoimmune diseases later.

The document likely offers guidance on treating a woman's excessive hair growth, considering her symptoms and obesity.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Scalp micropigmentation is a tattooing method that can mimic a full head of hair without surgery and has no healing time.

Babies who gain weight quickly, especially in the first 3 months, may start puberty earlier.

Different types of stem cells with unique roles exist in blood, skin, and intestines, and this variety is important for tissue repair.

Different women's hair and skin glands respond to hormones in varied ways, which can cause unwanted hair growth even with normal hormone levels, and more research is needed to treat this effectively.

Most children with CNS tumors on targeted therapy had skin reactions, which were generally treatable without stopping the therapy.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Children with atopic dermatitis often have sleep problems due to itching and may benefit from melatonin, which helps with sleep and skin symptoms.