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A baby boy had two types of temporary hair loss at birth, which might be two forms of newborn hair loss combined.

Hair loss can be a key sign of a rare type of rickets when vitamin D treatment doesn't work and advanced tests aren't available.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

Some children who had stem cell transplants developed permanent hair loss, especially when treated with a drug called busulphan.

Mice with the naked gene have missing or abnormal hair cells.

GAPO syndrome causes growth issues, hair loss, missing teeth, and vision problems.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Non-motor symptoms in myasthenia gravis are common and need early diagnosis for better management.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

A new syndrome may link skin, growth, mental, and hair issues.

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

The hairless gene mutation causes baldness by disrupting hair follicle structure.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

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

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Pili anulati may cause hair loss, proper diagnosis and treatment needed.

A girl with rickets and hair loss was found to have a rare condition where her body didn't respond to vitamin D treatment.

Pilomatricomas should be considered to avoid misdiagnosis in children with unusual skin tumors.

Triple H syndrome exists and can vary in symptoms.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Delayed puberty often runs in families, can affect growth, and may need hormone treatment.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

Patients with this syndrome can have different responses and worsening resistance to treatment over time.

A 38-year-old African American woman has a rare condition that prevents her from growing long hair.

Eyelash loss can temporarily occur from chemotherapy for retinoblastoma.

A possible link exists between minimal change nephrotic syndrome and complete hair loss.