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A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

Women with PCOS have distinct retinal changes compared to healthy women.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Routine eye exams may be needed for alopecia areata patients due to common eye issues.

Segmented hair color changes can indicate active alopecia areata.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

A woman lost vision in one eye after a forehead injection, but prompt treatment led to partial vision recovery.

The woman was diagnosed with Vogt–Koyanagi–Harada disease and successfully treated with medication, restoring her vision and stopping headaches.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

Finasteride, often used for hair loss, can potentially cause cataracts.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

Steroid use can cause a rare eye condition called central serous retinopathy, which can lead to permanent vision damage.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

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

Hair evaluation is crucial for early diagnosis and management of ARCI, as hair loss often indicates severity.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

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

Focal atrichia helps diagnose female pattern hair loss.

A young man had vision loss, hair loss, and other symptoms, but tests showed mostly normal results except for slightly high protein in spinal fluid.

Early diagnosis with trichoscopy can improve management and quality of life for CCCA patients.

Trichoscopy is useful for detecting and monitoring androgenetic alopecia.

AS-OCT is crucial for diagnosing VZV interstitial keratitis and avoiding unnecessary treatments.

A woman had eye pain and vision loss after a hair growth treatment, but her symptoms improved after a month.

A 20-year-old woman had stable Progressive Hemifacial Atrophy and Vitiligo after treatment, suggesting a possible link between the conditions.

Congenital atrichia with papular lesions causes permanent hair loss in children.

Early and accurate diagnosis of primary vitreoretinal lymphoma is crucial to prevent serious complications.