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A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

A 5-year-old boy has Nevus Comedonicus Syndrome, causing skin lesions and a cataract.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

A 4-year-old girl has a rare hair condition causing fragile, short hair.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

A 6-year-old boy developed excessive hair growth after taking diazoxide for low blood sugar.

TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

An adult with a rare skin condition improved with tazarotene treatment.

Dlx3 is essential for hair growth and regeneration.

Desmocollin 1 helps maintain skin structure during fetal development.

New mutations in the DSG4 gene cause a rare hair condition.

Hair follicle cells can help regenerate teeth.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

Dupilumab effectively treats severe skin issues in a rare genetic disorder.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Recognizing bamboo hair helps diagnose Netherton’s syndrome.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

The boy likely has a fungal infection causing hair loss.

Netherton's disease causes multiple hair defects.

Dental procedures and treatments show promise but need more research for conclusive results.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

Edar and Eda proteins are crucial for proper tooth development.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

A patient with Myotonic dystrophy type 1 had multiple tongue hemangiomas and was sensitive to anesthesia.