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

Scarring after cleft lip and palate surgery is a major issue, and the review looks at ways to manage it.

Scarring alopecias are a complex type of hair loss that are hard to treat and often can't be fixed with hair transplants.

Trichothiodystrophy causes unusual hair and developmental issues.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

The Covas-Lift is a safe and effective facial rejuvenation method with shorter surgery time and high patient satisfaction.

Tinea capitis can cause scalp issues in children and should be considered in similar cases; treatment with griseofulvin and selenium sulfide is effective.

Adolescents with PCOS have lower quality of life due to diagnosis, binge eating, and body image concerns.

A hairless patch on a boy's scalp from birth injury improved with minoxidil treatment.

Hair-shaft abnormalities can indicate neurological disorders, some of which are treatable.

A chest X-ray can effectively diagnose ectopic ACTH secretion from lung tumors.

A Japanese man with rare skin conditions improved with hydroxychloroquine treatment.

The study found that Short Anagen Syndrome results in short hair growth not due to hair fragility, and hair may grow longer after puberty.

Scalp cooling may be less effective for women of color on certain chemotherapy treatments.

Lupus can cause a type of hair loss that doesn't scar, due to inflammation.

Recognizing minor skin lesions can help identify serious cancer syndromes.

Calcitriol-resistant rickets is an inherited disorder that affects hair growth and causes hair loss.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

An 8-year-old boy with a scabies infection was successfully treated with permethrin, antihistamines, and antibiotics.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Early diagnosis and treatment of PCOS can prevent complications and improve symptoms.

Scalp psoriasis is treated with topical therapies, phototherapy, and systemic medications.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

Trichostasis spinulosa is a rare skin condition with hair-filled plugs in hair follicles.

Patients with central centrifugal cicatricial alopecia may have a higher risk of breast and colorectal cancer.

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

Early diagnosis and multidisciplinary care are crucial for managing PCOS in adolescents.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Skin problems after waxing led to a sarcoidosis diagnosis.

Early diagnosis and treatment of systemic-onset juvenile idiopathic arthritis are crucial for improvement.