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A 14-year-old girl with a condition that makes her hair easy to pull out also has a hair-pulling disorder, and treatment helped but she relapsed after a year.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Adolescents and young adults with Prader-Willi syndrome show a range of sexual interests and behaviors.

Lichen simplex chronicus on the scalp can be diagnosed by specific hair and skin signs and treated with corticosteroids and therapy.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Women with PCOS often feel anxious and distressed about their appearance, especially in social situations.

A new genetic variant of Woodhouse-Sakati syndrome was found in two adult sisters in Russia.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

Sheehan syndrome can cause hormone deficiencies after childbirth, but treatment can improve symptoms.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Rapunzel syndrome is more common in Asian countries and requires early diagnosis, especially in Asian girls.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Trichostasis spinulosa is a common but often unnoticed skin condition involving bundled vellus hairs, especially in people with darker skin or UV exposure.

Post-exposure syndromes are persistent conditions caused by past exposures, needing unique interventions.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Post-Exposure Syndromes are persistent conditions caused by past exposures, needing unique interventions.

A young girl with high testosterone was thought to have a tumor but actually had PCOS, which was treated with birth control pills.

Trichostasis spinulosa is a rare skin condition with hair-filled plugs in hair follicles.

Trichostasis spinulosa mainly affects the nose, with many tiny hairs in one follicle, possibly influenced by hormones and sunlight.

Two boys developed a viral skin infection during chemotherapy, which resolved with improved immune function.

Loose Anagen Syndrome is a hair condition where hairs can be easily pulled out, mainly affecting young girls, and may improve on its own or with treatment.

A rare hair follicle disorder can cause itchy, bluish-black bumps on the body.

Drospirenone can hide symptoms of certain hormonal disorders, complicating diagnosis.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.