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Topical rapamycin may effectively treat fibrous papules on the face.

A multidisciplinary approach with virtual sessions effectively reduces compulsive hair pulling in young people.

A rare case of isolated trichothiodystrophy was identified, marked by brittle hair with low sulfur content.

Oral Acitretin effectively resolved symptoms in a child with Netherton syndrome.

A five-year-old girl has a harmless, unchanging bald patch on her scalp.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Tofacitinib improved hair loss and skin symptoms in a patient after secukinumab caused hair loss.

An 80-year-old man with COVID-19 also had constrictive pericarditis, possibly due to an autoimmune or immunoglobulin related disease, and improved after surgery.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Ulerythema ophryogenes causes hair thinning and inflammation, with limited treatment options.

Recognizing and treating overlap syndrome in connective tissue diseases is crucial.

Hair bands are a new symptom of facio-genito-popliteal syndrome.

Brazilian keratin treatment can cause severe skin reactions.

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

Baricitinib improved nail condition and hair regrowth in a patient with alopecia and nail abnormalities.

Carbamazepine may cause reversible nail detachment.

Hidradenitis suppurativa tunnels worsen the disease and often need surgery because current treatments are not very effective.

KLHL24-mutant stem cells help understand skin and heart disease.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

Careful light microscopy is crucial for detecting mild cases of pili annulati, which weakens hair and varies widely in expression.

Localized trichorrhexis nodosa is a hair condition where hair becomes fragile and breaks easily due to damage.

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

Dermoscopy improves diagnosis and treatment planning for trichostasis spinulosa.

Diabetic patients often have ingrown nails due to obesity, high blood pressure, past injuries, bad nail trimming, nail fungus, weak foot pulse, and weak knee reflex.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Recognizing scalp symptoms in PRP is crucial for proper diagnosis and treatment.

Lower 2D:4D finger ratios in HS patients suggest prenatal hormone influence on the disease.

Sorafenib can cause rare skin reactions, but treatment can continue with additional care.