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This report describes a 6-year-old girl with Turner syndrome and coexisting psoriasis, alopecia areata, and trachyonychia, suggesting a potential link between these conditions.

In this report, two Persian cats and their owner with low immunity due to chemotherapy were identified with a rare dermatophytic infection caused by Chrysosporium spp., and the infection improved following fluconazole treatment.

This case report documents the second known instance of a salivary gland choristoma on the chest wall of a newborn, highlighting its benign nature and the importance of accurate diagnosis.

This case study found that a skin lesion in a Samoyed dog did not match any single known follicular cyst or neoplasm type described in the literature.

This case report describes a rare instance of thymoma associated with alopecia areata in a 60-year-old woman who had no signs of myasthenia gravis, highlighting the need for thoracic surgeons to consider alopecia in such cases due to its impact on quality of life.

This report describes a 23-year-old male with Clouston’s syndrome, characterized by nail abnormalities, palmoplantar skin thickening, anodontia, and androgenic alopecia, highlighting the need for supportive management due to the lack of a definitive treatment.

In this case study, a 69-year-old male with a neck swelling was diagnosed with a trichilemmal cyst, highlighting the importance of complete surgical excision for lesions with proliferative or malignant potential.

This study reports a case of ringworm in a Chinchilla lanigera, attributed to stress and contact with canine material contaminated with Microsporum canis.

This article discusses trichoscopy as a tool for differential diagnosis in female-type androgenetic alopecia and reports on three patient cases without providing new clinical results.

This report describes a patient with trichothiodystrophy exhibiting both specific hair abnormalities and developmental delay, contributing to the understanding of this rare disorder's clinical presentation.

This study diagnosed an 11-year-old girl with initial androgenetic alopecia and monilethrix after observing unique hair shaft abnormalities and skin conditions, unlike her affected parents.

This abstract presents a clinical case of a woman with traction alopecia and discusses trichoscopic findings without reporting any new research results.

This report presents the second known case of erythema nodosum without typical associated conditions, which could be linked to mycoplasma infection, although no testing was conducted to confirm this in the patient.

This report describes a case study of a 23-year-old female exhibiting multiple trichodiscomas, a type of benign tumor of the hair follicular discs common in familial cases and potentially linked to Birt-Hogg-Dube syndrome, though genetic testing was not performed due to financial constraints.

This article reports a case study of recurrent trichilemmal carcinoma of the scalp, highlighting its clinico-radiological and pathological features, along with its unique characteristics compared to other skin cancers.

This case report describes a unique occurrence of plica polonica in a lung adenocarcinoma patient on chemotherapy, linked to anagen effluvium from paclitaxel and carboplatin and uncustomary shampoo use.

This study observed that overexpression of Bcl-2 in certain transgenic mice accelerates catagen progression and increases hair follicle apoptosis and alopecia, while Bcl-2 deficient mice show delayed hair growth and pigmentation changes.

This study developed a chalcone-based molecule that significantly increased tyrosinase inhibition and solubility, showing potential as a safe and effective skin depigmenting and antiaging agent, with supportive epigenetic and antioxidant properties observed in vitro.

This case report describes a unique instance of congenital triangular alopecia affecting the chin in a 12-year-old boy, noting the condition is typically benign with limited treatment options being necessary.

In this study, Brca1(S971A/S971A) mice showed a moderately increased risk of spontaneous tumor formation and defects in DNA damage response, suggesting CHK2 phosphorylation of BRCA1 is crucial for tumor suppression.

In this case report, a 38-year-old woman with lifelong monilethrix and progressive frontal scalp thinning associated with androgenetic alopecia highlights the diagnostic and management challenges when these hair conditions coexist.

This review describes the dermatological uses of the contraceptive ethinylestradiol/chlormadinone acetate for conditions linked to high androgen levels and reports no new clinical results.

This case report describes the diagnosis of monilethrix in a 2-year-old boy using trichoscopy, highlighting its rarity and the challenge of diagnosing it without a family history.

This study suggests that immunohistochemistry of keratin and involucrin expression can aid in distinguishing malignant trichilemmoma from other tumors previously diagnosed as such.

This report highlights a case where intralesional cidofovir successfully treated squamous cell carcinoma without systemic toxicity, suggesting it may be a viable alternative to surgical excision.

This case study describes a 27-year-old woman with alopecia mucinosa that persisted for 20 years despite multiple treatments, including steroids and antihistamines.

This review discusses the pathogenesis of melasma, including genetic, environmental, and hormonal factors, and highlights potential avenues for new treatments and preventive strategies, but reports no new experimental findings.

This study found that chemotherapy for breast cancer initially reduced hair density and anagen hair rate, which then returned to baseline or higher, whereas tamoxifen did not significantly affect hair growth.

In this study, researchers found that CCCA in women of African descent is associated with molecular changes, including dysregulation of fatty acid metabolism and fibrosis pathways, suggesting potential targets for new treatments.

This study identified a high-risk allele in the PLCD1 gene associated with hereditary trichilemmal cyst formation, proposing a monoallelic two-hit mechanism as the underlying genetic pathogenesis.