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An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Onabotulinum toxin A may help treat trichotillomania and promote hair growth.

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

Surgery removed an ovarian tumor, improving her symptoms and normalizing testosterone levels.

Dermatologists should recognize diverse discoid lupus signs to avoid misdiagnosis.

New hair spray caused a hair shaft disorder.

Hidden sweat gland tumors might cause hair loss.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Sudden, unusual hair loss may indicate serious underlying health issues.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

Switching to a twice-weekly betamethasone treatment led to full hair regrowth in alopecia areata without side effects.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

PCOS affects nearly 25% of female medical and dental students, impacting their academic and social lives.

A 12-year-old boy in rural south India had a rare skin condition causing hair loss and inability to sweat.

A patient with a severe scalp burn developed chronic bone infection, treated with surgery and muscle-skin flap from the back.

Pediatric hair loss requires personalized treatment based on cause and severity, with specialist support.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

Minimally invasive glaucoma surgery can effectively manage glaucoma in GAPO syndrome when other treatments fail.

Hypothyroidism may cause vertigo symptoms like BPPV.

Early diagnosis and treatment of achalasia and hyperthyroidism improve patient outcomes.

A young Caucasian man experienced a rare type of hair loss on the back of his head.

Some drugs may increase the risk of obstructive sleep apnea, while others like certain biologics might decrease it.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

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