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Higher basal metabolic rate increases the risk of non-alcoholic fatty liver disease, especially in Chinese people, and may require tailored management.

Quick diagnosis and biotin treatment can dramatically improve biotinidase deficiency symptoms.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

Hair, skin, and nails supplement use nearly doubled from 2011 to 2020, with higher usage among young adults, females, and certain ethnic groups.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

The modified hair loss classification is more detailed but less user-friendly.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Including special area involvement helps identify more psoriasis patients who may need systemic treatment.

Forensic DNA phenotyping faces challenges due to inconsistent terminology, limited genetic understanding, and debates over technology and models.

Electron Beam Tomography (EBT) is a useful additional test to stress testing for detecting heart disease.

DNCB is highly effective for treating alopecia areata with minimal long-term side effects.

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

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Research on non-muscle invasive bladder cancer has increased, with the U.S. leading, and highlights effective treatments like BCG despite some side effects.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Despite progress, better treatments and understanding are needed for the high rates of long-term issues and deaths linked to eating disorders.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Consider amyloidosis in patients with specific nail changes and check for systemic issues.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

Lower illness acceptance is linked to more body dysmorphic disorder symptoms in patients with body modifications.

Sentinel lymph node biopsy is recommended for all types of desmoplastic melanoma due to higher rates of nodal metastasis.

Sentinel lymph node biopsy is recommended for all types of desmoplastic melanoma due to higher rates of nodal metastasis.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Recognizing the "bamboo hair defect" is crucial for diagnosing Netherton's syndrome.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.