Ruzicka Goerz Anton syndrome
|Ruzicka Goerz Anton syndrome|
Patient with Ichthyosis
|Classification and external resources|
Ruzicka Goerz Anton syndrome is a rare genetic disease described by Ruzicka et al. in 1981. It is characterized by icthyosis (rough, scaly skin), deafness, intellectual disability, and skeletal anomalies.
It is also known as "Ichthyosis deafness intellectual disability skeletal anomalies".
In 1981, a case was studied by Ruzicka et al. of a 15-year-old girl. The patient had ichthyosis congenita as well as deafness and retarded mental development. Further studies showed several skeletal deformities including brachydactyly, clinodactyly, and extra ribs. One year earlier, the patient had developed thyroid carcinoma, but whether or not this is due to the syndrome is unknown. The patient was treated with an oral retinoid, which greatly improved the patient's ichthyosis.
- "Ruzicka Goerz Anton syndrome". Check Orphan. Retrieved 2011-09-02.
- "Ruzicka-Goerz-Anton syndrome" (in Finnish). Mental Retardation Service Database. Retrieved 2011-09-01.
- "Ruzicka Goerz Anton syndrome". National Library of Medicine. 2010-08-25. Retrieved 2011-09-02.
- Ruzicka T, Goerz G, Anton-Lamprecht I (1981). "Syndrome of ichthyosis congenita, neurosensory deafness, oligophrenia, dental aplasia, brachydactyly, clinodactyly, accessory cervical ribs and carcinoma of the thyroid". Dermatologica 162 (2): 124–36. doi:10.1159/000250259. PMID 7250456.
- Tamayo, L.; Ruiz-Maldonado, R. (1980). "Oral retinoid (Ro 10-9359) in children with lamellar ichthyosis, epidermolytic hyperkeratosis and symmetrical progressive erythrokeratoderma". Dermatologica 161 (5): 305–314. doi:10.1159/000250382. PMID 6449393.
- Ruzicka Goerz Anton syndrome at the Genetic and Rare Diseases Information Center
- Causes of Ichthyosis at RightDiagnosis.com
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