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Type 3 5α-reductase is more common and finasteride and dutasteride strongly inhibit it.

New hair growth corticosterone levels are higher in diabetic mice, indicating long-term stress.

Insulin helps heal corneal wounds and nerves in diabetic mice by activating the Wnt signaling pathway.

Patients with Type 1 diabetes should be screened for pernicious anemia.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

Metformin improved menstrual cycle regularity and signs of hyperandrogenism in adolescent girls with type 1 diabetes but did not improve blood sugar control.

A girl with type 1 diabetes developed a serious eye condition very early, suggesting the need for earlier eye checks and that early treatment can work well.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

Vitiligo and alopecia areata might be early signs of Type 1 Diabetes.

Type 1 diabetes patients often have other autoimmune diseases, which complicate their care.

Type 1/17 inflammation in psoriasis increases skin cell growth due to a molecule that could be a new treatment target.

A young Saudi girl with uncontrolled type 1 diabetes and hypothyroidism had two rare conditions, Mauriac syndrome and Van Wyk–Grumbach syndrome.

Laser treatment shows promise for hair growth, but needs further research.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

People with PCOS have higher levels of PAI-1, which may increase their risk of heart disease and fertility issues.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Minoxidil improved hair growth in a child with a rare genetic disorder.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Exercise improves insulin sensitivity and hormone regulation in PCOS rats.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

In India, most patients with type 1 autoimmune polyglandular failure show symptoms in a specific order, starting with parathyroid gland issues, then yeast infections, and finally adrenal gland failure.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.