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Early diagnosis and hormone therapy can significantly improve outcomes for post-partum pituitary insufficiency in resource-limited settings.

Clinicians should be aware of alternating thyroid conditions and their treatment.

Skin can become dry and thick in hypothyroidism.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

A hidden autoimmune syndrome was found during a shock, showing thyroid, adrenal, and ovarian issues.

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

Severe insulin resistance can be managed with medication, lifestyle changes, and treatment for related conditions.

People with Down's syndrome often have more skin problems due to a weak immune system.

Laser hair-comb therapy doesn't improve male-pattern hair loss.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

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

The study concluded that there is no significant link between thyroid autoimmunity and alopecia areata.

Treating Netherton syndrome with growth hormone and dupilumab improves growth safely.

Trichothiodystrophy causes unusual hair and developmental issues.

The girl's thin hair was due to loose anagen syndrome, not other hair loss types.

The study found that alopecia areata and hypothyroidism increase the risk of each other, but androgenetic alopecia and hypothyroidism do not.

An infant developed excessive hair growth after a bone marrow transplant and cyclosporine treatment.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

A rare calcium deposit condition was found on a man's scalp.

RET mutation is important in familial medullary thyroid carcinoma, and BRAF mutation in papillary thyroid carcinoma is linked to more aggressive cancer and higher death rates.

Eyelash loss can be a sign of thyroid problems.

A 21-year-old had a rare developmental anomaly with a misplaced sebaceous gland in a hair follicle.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

A rare ovarian tumor caused early puberty signs in a 1-year-old girl, but surgery reduced hormone levels.

Hypothyroidism is most common in older females, with symptoms like weakness, weight gain, and hair loss.

Low free thyroxine (FT4) is common in young lupus patients and needs quick diagnosis and treatment.

Propylthiouracil, a thyroid medication, can cause skin blood clots and immune-related blood vessel inflammation.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

A woman with hypothyroidism developed an allergy to IV levothyroxine after being resistant to oral forms.

Finasteride's sexual side effects not caused by androgen deficiency or SRD5A inhibition.