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People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

The book details skin conditions in older adults, their link to mental health, cancer treatment importance, hair loss remedies, and managing autoimmune and itchy skin.

Adding celecoxib to chemotherapy improves survival and quality of life for gastric cancer patients with positive COX-2.

Parathyroid hormones are important for hair growth, but their use in treating hair loss from chemotherapy is still uncertain.

Benign skin tumors need accurate diagnosis to ensure proper treatment.

Alopecia areata, a common autoimmune hair loss condition, often runs in families.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

Familial frontal fibrosing alopecia affects premenopausal women too, and early diagnosis is important, but no proven medication exists yet.

Some families have a genetic condition where they are born with irregular scalp defects.

Eruptive vellus hair cysts can run in families.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Treatment with dutasteride, minoxidil, and artificial hair transplantation improved appearance but caused folliculitis.

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

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

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

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Frontal fibrosing alopecia has occurred in two related male families.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

HIV-positive pregnant women are more likely to experience severe bleeding, and a pregnant woman with familial hypertriglyceridemia had a successful early delivery with special care.

Two young siblings experienced hair loss without hormone issues or other skin problems.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

A girl inherited excessive body hair from her mother and grandmother.

The document concludes that the girl's hairlessness is likely inherited from her parents.

Premature hair graying in the face may be influenced by genetics and environment.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Newborn acne may be linked to family history of high male hormone levels.

Cantú syndrome may be linked to pituitary adenomas.