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Dr. Zitelli emphasized that "Mohs surgery" should only be called that when one doctor does both the surgery and pathology.

Hormonal therapies might help treat hidradenitis suppurativa, but treatment is complex and personalized.

A specific gene mutation causes Olmsted syndrome.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

The summary does not report the effectiveness of Stanozolol in treating Pityriasis rubra pilaris.

Topical corticosteroids are the main treatment for Erosive Pustular Dermatosis, but recurrence is common after stopping treatment.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

AI chatbots can help teach dermatology but need careful checking for accuracy.

The study concluded that careful examination is key to differentiate between lipidized fibrous histiocytoma and juvenile xanthogranuloma.

The study found that specific proteins are markers of hair follicle development in human fetuses.

Hormone therapy in transgender individuals can increase acne and affect hair growth and loss.

A pregnant woman with Werner's syndrome died during childbirth, but her baby survived and did not have the syndrome.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Acne can't be cured but can be managed with treatments like benzoyl peroxide and diet changes; it's costly and can lead to scarring and mental health issues.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

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

The document encourages attending the 2023 Dermatology Nurses' Association Convention.

Diphenyl cresyl phosphate has low toxicity but can harm the liver, kidneys, adrenal glands, and testicles at high doses.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Secondary syphilis in Cali, Colombia, shows high Treponema pallidum presence and challenges in early diagnosis, needing better public health strategies.

Oxidative stress plays a significant role in alopecia areata, and new treatments may include JAK inhibitors and antioxidants.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

Hair loss due to scarring can be treated by reducing inflammation, removing scar tissue, and transplanting hair. The Follicular Unit Extraction technique is effective but requires skill and time. Future focus should be on scar-less healing methods.

A young man's hair loss was the only sign of syphilis, which improved after treatment.

Understanding how acne develops in different diseases could lead to new treatments.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

The study suggests fibrosing alopecia in a pattern distribution has distinct features and may vary by race.