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Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Doxazosin mesylate and saw palmetto cause genetic changes in fruit flies.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

Skin patterns form through molecular signals and genetic factors, affecting healing and dermatology.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

A one-year-old child with a genetic condition had symptoms improved by treating zinc deficiency.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

The document is a detailed medical reference on skin and genetic disorders.

Finasteride may cause lasting sexual and mental health issues, and genetic screening could help prevent them.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.