Nakajo syndrome is a rare congenital disorder reported in 1939 by A. Nakajo in the offspring of consanguineous (close blood relative) parents. Characteristics of the syndrome include erythema, loss of body fat in the upper part of the body, and disproportionately large eyes, ears, nose, lips, and fingers.[1]
| This genetic disorder article is a stub. You can help Wikipedia by expanding it. |
References
This entry is from Wikipedia, the leading user-contributed encyclopedia. It may not have been reviewed by professional editors (see full disclaimer)




