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The top research priorities for congenital ichthyosis include long-term side effects of oral retinoids, best topical treatments, and treatments for itch and hair loss.

Two Australian Poll Hereford calves had severe anaemia, abnormal red blood cells, and skin issues.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Accurate diagnosis of basaloid follicular hamartoma is crucial to avoid unnecessary treatments.

A hereditary condition causes hair loss and twisted hair in some family members.

Congenital atrichia is a rare condition where children are born without hair, and treatment is often ineffective.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

An 8-year-old girl had a rare, benign skin tumor on her forehead.

Congenital triangular alopecia can occur outside the typical fronto-temporal region.

A rare skin condition with cysts was found on a 5-year-old boy's scalp.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

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

Congenital triangular alopecia is more common than thought and some treatments can be beneficial for appearance concerns.

Hair steroid measurement is an effective method to diagnose and monitor CAH in developing countries.

Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

FOXN1 duplication can cause excessive hair growth.

A man with a birthmark on his scalp developed hair loss that improved with treatment, but the link between the birthmark and hair loss was unclear.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

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

Inhaled substances in e-cigarettes can cause hormone imbalances similar to congenital adrenal hyperplasia.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

The junction of the inner and outer prepuce with good blood flow is ideal for surgical flaps.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

A single recessive gene causes sparse hair in certain Japanese White rabbits.

A 6-year-old Asian boy has a rare scalp condition causing hair loss and thickening, with unclear causes and no effective treatment.

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

Diagnosing simple-virilizing congenital adrenal hyperplasia can be difficult and requires thorough testing and expert advice.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.