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Children with frequent severe infections and low antibodies should be checked for immune deficiencies.

Inhibiting SFRP1 may help treat hair loss.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

ALP and ACP have different roles in dog skin, with ALP aiding growth and maintenance, and ACP involved in breakdown processes.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Targeting CXXC5 and GSK-3β may help treat male pattern baldness.

Prolactin contributes to hair loss by promoting hair follicle shrinkage and cell death.

Hair transplants can trigger a rare scarring hair loss that is hard to treat.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Genetic variants in specific genes cause a type of hair loss.

Farudodstat may effectively treat alopecia areata without harming hair follicles.

PFD patch helps laser tattoo removal, trichoscopy diagnoses AGA, and serum boosts SOD activity.

Genetics, low estrogen, and low iron levels contribute to female hair loss, with specific scalp signs indicating severity.

ILC1 cells contribute to hair loss in alopecia areata.

Recognizing mild or atypical cases of ectodermal dysplasia is crucial for better treatment and future planning.

Lichen planopilaris (LPP) is linked to androgen excess, while frontal fibrosing alopecia (FFA) is linked to androgen deficiency.

Females with 5 alpha-reductase-2 deficiency have less body hair, no acne, normal fertility, and delayed menarche.

A woman's hair loss was correctly diagnosed as Lichen planopilaris after initial misdiagnosis, highlighting the usefulness of trichoscopy in diagnosing hair disorders.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Four new FGF5 gene variants cause long hair in dogs.

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

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.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.