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Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

In teens with Polycystic Ovary Syndrome and obesity, issues related to metabolism, skin, and mental health are common, and a clinic with various specialists can provide care for most of these problems.

Irregular menstrual cycles in teenagers are linked to a higher risk of polycystic ovary syndrome and metabolic syndrome.

Adolescents and young adults with Prader-Willi syndrome show a range of sexual interests and behaviors.

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

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Hair changes can indicate systemic diseases or medication effects.

P-selectin is not the only factor that prevents scarring in fetal wound healing in mice.

Washing baby socks without flipping them inside out may increase the risk of Hair Tourniquet Syndrome.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

To improve use of the contraceptive DMPA among adolescents, effectively manage side effects like menstrual changes and weight gain through counseling and guidance.

Early diagnosis and treatment of PCOS in teenagers can help prevent more severe adult PCOS.

New genetic mutations linked to rare skin disorders were found in three newborns.

Penile strangulation from hair can cause severe harm but can be treated if caught early.

Metformin improved menstrual cycle regularity and signs of hyperandrogenism in adolescent girls with type 1 diabetes but did not improve blood sugar control.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Hair removal cream effectively and painlessly treated infants with hair tourniquet syndrome.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

A boy with toxic shock syndrome had severe heart rhythm problems but recovered with treatment.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

Child with rickets improved with a specific vitamin D therapy, but alopecia did not change.

Recurrent vaginal bleeding in young girls without puberty signs may require a genital exam to find hidden causes.

The girl with autoimmune hair loss might regrow hair within a year, and treatments can help but not prevent recurrence; dermatologist referral and corticosteroids are recommended.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

In India, most patients with type 1 autoimmune polyglandular failure show symptoms in a specific order, starting with parathyroid gland issues, then yeast infections, and finally adrenal gland failure.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.