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A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

A rare case linked complete hair loss to both pancreas and gallbladder cancer.

A postmenopausal woman's hirsutism and high testosterone levels improved after surgery for an ovarian tumor not seen on ultrasound.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

A rare case of lupus linked to thymoma shows complex diagnosis and management challenges.

Topical glycopyrrolate lotion helped reduce excessive sweating from eating in a diabetic man.

Early diagnosis, intensive therapy, and careful follow-up are crucial for managing overlapping TTP and SLE.

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

Dermoscopy improves diagnosis and treatment planning for trichostasis spinulosa.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.

Short anagen syndrome causes short hair that may grow longer after puberty.

A person with Werner syndrome was initially thought to just have female pattern hair loss.

Trichotillomania can be identified by a "Friar Tuck sign" and nail-biting.

Trichoscopy is crucial for diagnosing rare genetic hair disorders.

A gluten-free diet and removing the parathyroid adenoma helped a girl with coeliac disease and high calcium levels start puberty.

A rare skin condition usually on the face was found on a man's heel.

A 7-year-old girl was diagnosed with Netherton's Syndrome, shown by skin and hair symptoms.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

A PET-CT scan successfully located a hard-to-find Leydig cell tumor in a woman with hormonal symptoms.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A 14-year-old girl with Loose Anagen Hair Syndrome was successfully treated with oral Minoxidil and a Silicon supplement.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

Shrinking of oil glands in the skin is a key sign of hair loss linked to TNF inhibitor drugs and may improve if the treatment is stopped.

Lupus enteritis is a rare but serious gut inflammation in lupus patients, often hard to diagnose without prior lupus symptoms.

A woman's masculine symptoms were caused by an ovarian tumor, which improved after surgery.

Finasteride may effectively reduce Tourette's syndrome symptoms and improve life quality.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Hair-thread Tourniquet Syndrome, where hair or thread tightly wraps around a body part, is not rare and requires early detection to prevent serious damage.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

Tick-bite alopecia can be identified by a bite-centered mark and treated with topical steroids, while SENLAT needs doxycycline.