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A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

Cepharanthine may help treat lung fibrosis by affecting certain immune cells.

The conclusion is that hair loss from CCCA may be genetic and not solely caused by hair grooming practices.

Cetuximab can cause excessive eyelash growth.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Dissecting cellulitis of the scalp mainly affects Black males and requires early diagnosis and management.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Panitumumab can cause excessive ear hair growth.

A rare family case of multiple benign hair follicle tumors was identified, highlighting the need to distinguish them from similar conditions.

The Foxn1 gene is essential for normal nail and hair development.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

Uncombable hair syndrome causes dry, frizzy hair that can't be combed flat, seen in a young child.

Germacrone from Curcuma aeruginosa may help treat conditions related to male hormones by blocking a specific enzyme.

A deer fawn in South Dakota was the first cervid found with congenital hypotrichosis, a condition causing sparse or missing hair.

Early diagnosis and treatment of NCCAH can improve symptoms and fertility.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

The research mapped diverse cell types in mouse lacrimal glands, aiding understanding of gland biology and diseases.

A French bulldog had sparse hair due to a condition similar to that seen in Chinese crested dogs.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

A new compound from a sponge strongly inhibits an enzyme linked to male-pattern hair loss without being toxic at low levels.

CRH can cause hair loss by promoting cell death in hair growth cells.

Idiopathic chronic telogen effluvium in women causes sudden hair loss without a known cause, often linked to emotional distress.

The fuzzy gene is crucial for controlling hair growth cycles.

A rare skin tumor with extra hair growth was found and safely removed from a 27-year-old woman.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

NuMA-microtubule interactions are crucial for proper skin structure and hair growth.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.