Search

everythinglearnresearchcommunity

for

Search:↓

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Overt hyperthyroidism is the most common thyroid disorder, especially in women.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Recognizing macro-TSH is crucial to avoid unnecessary treatments.

High prolactin levels can cause skin and hair symptoms similar to those caused by hormone imbalances.

A 33-year-old woman with PCOS and metabolic syndrome was unusually diagnosed with a bone condition called DISH, suggesting a possible link between these conditions.

A rare adrenal tumor in a woman only made DHEA-S, causing hair thinning, and was removed, fixing the hormone level.

Homeopathy improved hypothyroidism symptoms in a 27-year-old woman.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Human scalp hair follicles can produce hormones and have a system similar to a brain-body communication network.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Idiopathic hirsutism might not be truly idiopathic but could be an early stage of hyperandrogenic disorders.

A specific mutation in PA-PLA1α causes abnormal hair growth.

Hyperthyroidism can hide signs of high androgen levels in females.

A newborn girl had a rare case of salivary gland tissue on her chest, which was safely removed.

Calcitriol-resistant rickets is an inherited disorder that affects hair growth and causes hair loss.

A woman with Hashimoto's hypothyroidism developed Graves' hyperthyroidism after 20 years, showing these conditions may be linked.

A rare ovarian tumor caused high male hormone levels, but surgery fixed it.

Surgical removal of an adrenal tumor resolved hormonal issues in a young woman.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

PAON shows skin patterns due to genetic mosaicism.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.

Hypothyroidism and hyperprolactinemia may cause hair loss in women.

Different growth patterns in thyroid tumors are influenced by where cell growth and death occur.

A rare skin growth in a baby was successfully removed without coming back.

Abnormal adrenal function is not the cause of alopecia in Pomeranians; it may be due to breed-specific hormones.

ACTH-dependent Cushing's syndrome linked to metastatic cervical cancer is rare and has high risks.

A 3-year-old boy lost all his hair due to a rare reaction to phenobarbital, but it grew back after steroid treatment.