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New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Crossbreeding certain European cattle breeds may cause hair and physical issues in cattle.

Measuring 17-hydroxyprogesterone in hair can help monitor androgen levels in people with congenital adrenal hyperplasia.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

A genetic marker linked to a type of hair loss was found in most patients studied.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

Ectopic adrenal rests can cause androgen excess after adrenalectomy and may need targeted surgery.

Women with congenital adrenal hyperplasia showed no prostatic growth.

A newborn with congenital syphilis had unusual hair loss possibly caused by the infection.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

New genetic mutations linked to rare skin disorders were found in three newborns.

Acitretin helped improve hand mobility and skin condition in a patient.

Untreated Congenital Adrenal Hyperplasia can cause severe hair loss due to high androgen levels.

Women with congenital adrenal hyperplasia (CAH) have more sexual function issues than those with polycystic ovary syndrome (PCOS), but physical activity can improve sexual functioning in all women.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

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.

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

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

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.

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.