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Miliacin helps damaged hair follicles grow new hair faster.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

The study found certain scalp biopsy features can help tell apart alopecia areata from pattern hair loss even when typical immune cells are not seen.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Yellow dots look different in various hair loss conditions and can help diagnose them.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

The document is a detailed medical reference on skin and genetic disorders.

The author clarifies that alopecia areata incognito and diffuse alopecia areata are different types of hair loss with unique symptoms and challenges in diagnosis.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

The patient's hair loss is most likely due to diffuse alopecia areata.

Dermoscopy helps accurately diagnose temporal triangular alopecia, avoiding unnecessary treatments.

Other common signs, not just the well-known immune cells around hair bulbs, are important for diagnosing hair loss from alopecia areata.

The research found specific signs to diagnose alopecia areata incognito and noted patients generally regrow hair after steroid treatment.

Dermoscopy helps diagnose different types of hair loss and may reduce the need for biopsies.

A woman's hair loss during Hepatitis C treatment with PEG-INF-a-2a and Ribavirin was reversible after stopping the medication.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

Trichoscopy can effectively tell apart tinea capitis and alopecia areata in children by looking for specific hair shapes.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Syphilis can cause hair loss without other symptoms and should be considered when diagnosing unexplained hair loss.

The conclusion introduces a new way to classify skin cysts using their shape and genetic markers.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Masculine facial features may not reliably indicate heritable health, and more research is needed.

Dermoscopic and histopathological features combined can help diagnose Pityriasis versicolor.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

Temporal triangular alopecia in infants is mostly seen in males at birth, with unique features that help with diagnosis.

Dermoscopy is a useful tool for identifying features of skin conditions, but more research is needed to define its role in dermatology.