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The patient has a rare skin condition that shows features of two known disorders.

Dermoscopy helped diagnose a rare skin disease which slightly improved with treatment.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

A woman with a rare scalp infection was cured after one month of medication.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Isotretinoin effectively treated a rare scalp condition, but careful drug monitoring and a dairy-free diet were important.

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

A woman's rare benign eyelid tumor was correctly identified through detailed tissue analysis.

The woman has a rare, harmless skin condition specific to pregnancy that causes itchy bumps and will go away after she gives birth.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Trichofolliculoma, a rare benign hair follicle tumor, can potentially recur.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

A woman with a rare scalp condition causing a thick scalp and hair loss didn't improve with steroid treatment.

A 23-year-old woman's missed periods were caused by a rare genetic disorder treated with hormone patches.

A woman with a rare ovarian tumor and hyperparathyroidism improved after surgery, highlighting the need for reporting unusual cases to understand and manage rare diseases.

A child with a rare scalp condition regrew hair after treatment.

Plica polonica is a rare condition where hair becomes irreversibly tangled, and the treatment is to cut the matted hair.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

Hair matrix cysts are rare skin nodules with unique features, often needing surgical removal.

EPDS is a rare, chronic scalp condition that's hard to treat and needs better awareness for improved outcomes.

Folliculitis decalvans is a rare skin disease causing hair loss and requires personalized treatment.

Kerion is a rare but serious scalp infection that needs proper treatment.

The cat had a rare condition linked to cancer, leading to its euthanasia.

A man developed a rare late-onset hair-pulling disorder, usually seen in younger people.

Some goats get rare skin diseases from not enough vitamin E, selenium, or zinc, but they're usually still healthy.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

A toddler with a rare adrenal gland tumor causing male-like physical changes was successfully treated with surgery.

Monilethrix is a rare genetic hair disorder with no cure, but low-dose oral minoxidil may help.

A cat with a rare pancreatic tumor and diabetes died despite treatment, showing similar symptoms to a human condition.

A cat had a rare skin disorder with hair loss and scaling, linked to a suspected tumor.