Follicular atrophoderma

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Follicular atrophoderma
Synonyms
Pronounce N/A
Specialty Dermatology
Symptoms Follicular depressions, keratosis pilaris
Complications
Onset
Duration
Types N/A
Causes Genetic disorder
Risks
Diagnosis Clinical diagnosis, skin biopsy
Differential diagnosis Keratosis pilaris, Ichthyosis
Prevention N/A
Treatment Emollients, keratolytics
Medication
Prognosis
Frequency Rare
Deaths N/A


Follicular Atrophoderma is a rare skin condition characterized by the presence of small, depressed, follicular-based pits. It is often associated with other skin abnormalities and systemic symptoms.

Symptoms[edit]

The primary symptom of Follicular Atrophoderma is the presence of small, depressed, follicular-based pits. These pits are typically less than 1 mm in diameter and are most commonly found on the face, arms, and legs. Other symptoms may include hair loss, skin atrophy, and hyperpigmentation.

Causes[edit]

The exact cause of Follicular Atrophoderma is unknown. However, it is believed to be a genetic disorder, as it often runs in families. Some researchers believe that it may be caused by a mutation in the BMP1 gene.

Diagnosis[edit]

Diagnosis of Follicular Atrophoderma is typically made based on the characteristic appearance of the skin. A skin biopsy may be performed to confirm the diagnosis.

Treatment[edit]

There is currently no cure for Follicular Atrophoderma. Treatment is typically focused on managing the symptoms and may include the use of topical steroids, retinoids, and laser therapy.

Prognosis[edit]

The prognosis for individuals with Follicular Atrophoderma varies. Some individuals may experience a slow progression of the disease, while others may experience a rapid progression. The disease does not typically affect life expectancy.

See Also[edit]

References[edit]