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New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

Girls with Autism Spectrum Disorder may show different symptoms than boys, leading to missed or delayed diagnoses.

Most clinicians follow discharge guidelines, many lupus patients don't use sunscreen regularly, dithranol is effective for psoriasis, biopsy methods should be based on lesion type, voriconazole may raise skin cancer risk, a new scale can help diagnose female hair loss early, and most melanomas may develop from existing moles.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Accurate diagnosis of cicatricial alopecias requires thorough scalp examination and multiple biopsy techniques.

Low-dose acitretin helps nail psoriasis, stem cells may treat scarring alopecia, Chinese men have lower baldness rates, lateral foldplasty is good for ingrown toenails, hair diameter helps diagnose female baldness, childhood trauma linked to alopecia areata, certain hair-weaving leads to scalp conditions in African American women, and new methods for hair research and understanding hair and sweat gland development were introduced.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

Older adults have a high rate of skin cancers like basal cell carcinoma and melanoma, mainly due to UV exposure and age.

Children's screen time increased during the pandemic, causing various health issues.

Passiflora incarnata may help with anxiety but has risks and drug interactions. There's a genetic link between Fragile X Syndrome and Autism Spectrum Disorder. 6.7% of urine cultures showed hospital-acquired urinary tract infections. Children used screens more during COVID-19, causing various health complaints. Autism Spectrum Disorder is often underdiagnosed in females. Dissociative disorders in childhood sexual abuse victims are more common in males. Most pregnant teenagers are not dissatisfied with their body image but worry about weight. Diagnosing tuberculosis after knee surgery is challenging due to non-specific symptoms. Post-COVID-19 syndrome is more common in older, severely affected patients. Psychiatrists should be part of pain management teams due to the psychological aspects of pain.

The transcription factor Meis2 is essential for touch sensation and proper nerve development in touch receptors.

Hair transplantation can improve scars after removing a rare skin cancer.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Metformin and liraglutide improved symptoms of HAIR-AN syndrome in a child.

A baby had a rare case of widespread milia, which was treated and is being monitored.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A Chinese boy's scalp infection from a guinea pig was cured with medication.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

An adult woman with scalp infection recovered after antifungal treatment, with no return of symptoms.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A woman in Turkey with a scalp infection was cured using oral and topical antifungals after a recurrence due to not following the treatment properly.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

CGF therapy may effectively treat psoriasis by reducing inflammation.