Haber syndrome
Haber Syndrome
Haber Syndrome (pronounced: /ˈhɑːbər/), also known as Haber's Syndrome, is a rare genetic disorder characterized by a variety of skin abnormalities, eye disorders, and dental anomalies. The syndrome was first described by the dermatologist Ralph C. Haber in 1976, hence the name.
Etymology
The term "Haber Syndrome" is derived from the name of the dermatologist Ralph C. Haber, who first described the condition in a medical journal in 1976. The word "syndrome" comes from the Greek "σύνδρομον" (syndromon), meaning "concurrence of symptoms," or "running together."
Symptoms
Haber Syndrome is characterized by a variety of symptoms, including:
- Cutaneous abnormalities: These include acne, rosacea, and seborrheic dermatitis.
- Eye disorders: These may include cataracts, glaucoma, and keratoconus.
- Dental anomalies: These may include malocclusion, hypodontia, and microdontia.
Diagnosis
Diagnosis of Haber Syndrome is typically based on the presence of the characteristic symptoms. Genetic testing may also be used to confirm the diagnosis.
Treatment
Treatment for Haber Syndrome is typically symptomatic and supportive. This may include dermatological treatments for skin abnormalities, ophthalmological treatments for eye disorders, and dental treatments for dental anomalies.
See also
References
External links
- Medical encyclopedia article on Haber syndrome
- Wikipedia's article - Haber syndrome
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