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Protein analysis shows aging changes in scalp cell types from women.

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

Skin aging and cancer development are influenced by the competition between stem cells.

Low oxygen levels affect the behavior of certain proteins in human skin cells.

Human-induced stem cell-created skin models can help understand skin diseases by studying the skin's layers.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

A one-year-old cat had multiple benign skin tumors similar to those known in humans.

A baby had a rare case of widespread milia, which was treated and is being monitored.

Lichen planopilaris causes permanent hair loss and scarring due to damage to hair follicles and can be mistaken for other hair loss conditions.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Different genes are linked to various types of hair loss.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

A condition called Central Centrifugal Cicatricial Alopecia causes hair loss and scalp burning in middle-aged African women, and it's treated with various medications, hair transplants, and non-drug methods like wigs.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

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

Growth hormone levels affect hair growth and loss, with too much causing excess hair and too little leading to hair loss.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Thyroid disease can cause skin, hair, and nail problems, and treating the thyroid condition often improves these symptoms.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.