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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

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A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

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CARASIL can cause different symptoms even with the same genetic mutation.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Gene sequencing is essential for diagnosing Junctional epidermolysis bullosa.

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The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Risankizumab effectively treats and maintains skin clearance in moderate-to-severe psoriasis.

Manfred Lucas, MD, lived from 1938 to 1997.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Errors found in identifying furosemide and finasteride polymorphs due to incomplete data.

Most patients successfully switched from the original adalimumab to a biosimilar with few reverting due to reduced effectiveness or side effects.

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The DMI3 gene is essential for nodule development and symbiosis in certain plants.

WS PRO 160 I 120 mg effectively treats urinary symptoms from BPH with good safety and tolerability.

Lactobacillus paracasei HY7015 helps hair grow in mice.

Narrowband-UVB phototherapy successfully treated a rare case of Graham Little-Piccardi-Lassueur syndrome.

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The method accurately measures Tamsulosin and Finasteride in medication and is suitable for regular quality checks.

Rice husk and bran extracts from the Bue Bang 3 CMU variety can potentially treat hair loss due to their antioxidant, anti-inflammatory, and anti-androgenic properties.