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Different types of hair loss in dogs and cats have various causes and treatments, with outcomes ranging from good to uncertain.

The conclusion is that different types of hair loss in dogs and cats can be cosmetic or serious, and affected animals should not be bred.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

EPR spectroscopy showed that spontaneous hair growth results in thicker skin and less pigmented hair than depilation-induced growth.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Chesapeake Bay retrievers' hair loss is likely a breed-specific, hereditary condition linked to abnormal steroid levels and distinct skin changes.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

Many elderly women experience unwanted facial hair and various hair loss conditions, with treatments available for each condition.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Certain groups may need vitamin supplements to improve hair health and prevent other health problems.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

All-trans retinoic acid causes hair loss by increasing TGF-β2 in hair follicle cells.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

The document explains the genetic causes and characteristics of inherited hair disorders.

The review concludes that accurate diagnosis of different types of hair loss requires proper biopsy techniques and understanding the hair growth cycle and underlying causes.

The conclusion is that detailed clinical descriptions help pathologists diagnose hair loss conditions more accurately.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Oral minoxidil shows promise in treating monilethrix-related hair loss.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Understanding fetal skin development helps diagnose congenital skin diseases.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Mutations in the LSS gene cause a rare type of hereditary hair loss.