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An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

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

Thymosin beta 4 protects cells from damage by blocking a harmful microRNA and boosting a protective gene.

Early recognition and multidisciplinary management of Whitaker syndrome can improve patient outcomes.

Spironolactone may help enlarge a small breast linked to Becker's nevus.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

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

Trichothiodystrophy can be linked to urologic issues and high calcium in urine.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

A 23-year-old man has a benign, non-progressive hair loss patch that doesn't respond to treatment but can be cosmetically treated.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The hamartoma is an abnormal hair growth with limited development in the upper hair follicle.

Hormone-replacement therapy improved a woman's skin condition known as lymphomatoid papulosis.

Triple H syndrome exists and can vary in symptoms.

Trichoscopy effectively diagnoses temporal triangular alopecia in children.

Early diagnosis and treatment of TPP can prevent complications.

Removing Sprouty genes in mice causes various hormone-related issues but does not increase cancer risk by one year of age.

A rare adrenal gland tumor can cause unusual symptoms due to hormone changes.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

Polythelia pilosa is a type of extra breast tissue with hair and should be classified as such.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

A 15-year-old girl with rare reproductive disorders received hormone therapy to develop secondary sexual traits, but infertility persisted.

Higher thyroid antibodies in Hashimoto's thyroiditis are linked to more inflammation and symptoms.

Subclinical hypothyroidism in women with PCOS affects thyroid and hormone interactions but not ovary structure.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.