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Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

The study found genetic variations in sheep linked to traits like milk production, growth, and health.

SCAD can indicate ANA-negative lupus, especially in women with unusual symptoms.

Low free thyroxine (FT4) is common in young lupus patients and needs quick diagnosis and treatment.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

PNH can occur in patients with SLE, so doctors should be aware of this.

Patients with limited English prefer professional language interpretation in otolaryngology clinics.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

The MTR gene affects wool quality and production in Chinese Merino sheep.

SLE symptoms in Dubai are similar to those in other Arab and Western countries.

Digital gangrene can be a rare first sign of late-onset systemic lupus erythematosus.

MK-0773 is a moderate inhibitor of the SRD5A2 enzyme.

A 13-year-old girl was diagnosed with juvenile lupus, showing only hair loss as a symptom.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

lncRNAs may regulate hair follicle development in Hu sheep.

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

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

Costovertebral arthritis can cause chronic back pain in SLE patients and needs thorough evaluation.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

GI197111X is best dissolved in Capmul MCM for trials.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

The CORIN gene variant causes the golden color in Siberian cats.

Macrophage activation syndrome can be a deadly first sign of systemic lupus erythematosus.

The mRNA-1273 COVID-19 vaccine may worsen symptoms in people with systemic lupus erythematosus.

A Japanese man with rare skin conditions improved with hydroxychloroquine treatment.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

SLHA can be hard to diagnose and needs teamwork between specialists.

A mutation in the VDR gene affects hair cycling without needing ligand binding.