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Patients with Complete Androgen Insensitivity Syndrome need psychological support and multidisciplinary care for complex treatment decisions.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

The ferret had hyperadrenocorticism and other health issues like heart, liver, and kidney problems.

Ichthyosis serpentina may be a variant linked to bamboo hair, with a possible genetic component.

Congenital Adrenal Hyperplasia is mainly caused by enzyme deficiencies, leading to varying symptoms like hormone imbalances and physical changes.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

Björnstad syndrome causes twisted hair from birth.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Rosella C. believes an earlier diagnosis of Cushing disease could have prevented severe symptoms.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Early intervention and protective measures are crucial for managing CIPA due to the lack of pain and standard treatment.

PCOS causes symptoms like irregular periods, acne, and infertility, needing careful diagnosis.

Early diagnosis and treatment of NCCAH can improve symptoms and fertility.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

A 39-year-old woman developed uncombable hair syndrome after taking oral contraceptives.

MIS-A is a severe complication after COVID-19, mostly in young black males, needing more research and awareness.

Long COVID patients have more health issues than non-infected people.

Cyclosporine-A can cause excessive hair growth, which usually stops after discontinuing the drug.

A rare pituitary tumor in an 18-year-old male caused hormonal issues and vision loss, requiring surgery and further treatment.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

Somatostatin analogues effectively manage ectopic ACTH syndrome when surgery isn't possible.

Most patients with Central Centrifugal Cicatricial Alopecia at the reviewed institution were middle-aged Black women, often with no symptoms, and commonly treated with topical medications.

PCOS care in Singapore can be bettered by refining referral systems, standardizing diagnosis and treatment, enhancing complication screening, and offering educational resources for clinicians.