Search

everythinglearnresearchcommunity

for

Search:↓

A girl initially thought to have a psychiatric disorder was later found to have a lupus-related condition, which improved with proper treatment.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

A man with itchy skin lesions and weight loss was diagnosed with a rare skin condition linked to a pancreatic tumor.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

A hair strand caused a rare case of limb strangulation in a teenage girl with autism, and the condition is not always linked to child abuse.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

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

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Acitretin significantly reduced inflammatory attacks in a woman with Naevus Comedonicus Syndrome but caused side effects.

Celiac disease patients often have psoriasis, dermatitis herpetiformis, and alopecia areata, but rarely vitiligo.

Dermatologists should consider congenital syndromes like TRPS in young adults with early hair loss.

A 5-year-old girl with McCune-Albright syndrome grew abnormal hair due to the drug tamoxifen.

A rare skin condition in a 17-year-old was diagnosed late, stressing the need for careful evaluation and genetic testing.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

Accurate diagnosis of rare pilomatrix carcinoma is crucial for effective treatment.

Most children with MIS-C showed significant improvement by 6 months.

Elderly patients with eruptive skin bumps may have clear cell syringoma linked to glucose issues.

Trichoscopy can diagnose Netherton syndrome without pulling hairs.

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

Timely and aggressive treatment is crucial for improving outcomes in severe complications of adult-onset Still's disease.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

CCCA mainly affects Black women and is linked to high-tension hairstyles, heating tools, chemical relaxants, and genetics.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

Certain factors can trigger hormonal imbalances and cyst formation, leading to Polycystic Ovarian Syndrome (PCOS).

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Selenium deficiency can cause skin and hair color loss, muscle weakness, and blood cell changes, but these improve with selenium supplements.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.