A newborn girl is described with the following multiple congenital anomalies: an orbital cyst, cutaneous appendages, focal hypo-aplasia of the skin and multiple cerebral cysts. This case of oculo-cerebro-cutaneous syndrome is compared with four previously published cases.
Hemifacial myohyperplasia: Description of a new syndrome
โ Scribed by Lee, Samson ;Sze, Raymond ;Murakami, Craig ;Gruss, Joseph ;Cunningham, Michael
- Book ID
- 101317459
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 313 KB
- Volume
- 103
- Category
- Article
- ISSN
- 0148-7299
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โฆ Synopsis
Hemifacial hypertrophy is a rare condition characterized by unilateral enlargement of all tissues of the face. We describe three patients who exhibit hemifacial hyperplasia of the muscles of facial expression with no other organ system involvement. These three cases, in addition to six other cases identiยฎed in the literature, describe a unique constellation of characteristics that place these patients into a distinct syndrome. We suggest that the term ``hemifacial myohyperplasia'' be used to describe this speciยฎc and unique condition.
๐ SIMILAR VOLUMES
## Abstract We report on a sporadic case of hemifacial hamartomatous hyperplasia. The patient is male, and has sebaceous nevusโlike skin change, subcutaneous lipomatous mass, cranial bone hyperplasia, and bony change of meninges. His lesion involves the anterior half of the face and cranial base, a