Neurofibromatosis with fully expressed Noonan syndrome
- 1 April 1988
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 29 (4), 937-941
- https://doi.org/10.1002/ajmg.1320290426
Abstract
We present an 18‐year‐old man with neurofibromatosis (NF) and classic manifestations of the Noonan syndrome (NS), including the cardiac findings. His father also has neurofibromatosis but only some of the characteristics of Noonan syndrome. This case lends further support to the notion that the neurofibromatosis‐Noonan syndrome (NF‐NS) is a discrete entity and demonstrates that the NF‐NS can be inherited, with variable expression of the Noonan phenotype within a family.Keywords
This publication has 9 references indexed in Scilit:
- Evidence that the “neurofibromatosis‐Noonan syndrome” is a variant of von Recklinghausen neurofibromatosisAmerican Journal of Medical Genetics, 1987
- Vertical transmission of the neurofibromatosis/Noonan syndromeAmerican Journal of Medical Genetics, 1987
- Noonan's syndrome and neurofibromatosis.Archives of Disease in Childhood, 1987
- Noonan syndrome.Journal of Medical Genetics, 1987
- Congenital lid ptosis associated with neurofibromatosisAmerican Journal of Medical Genetics, 1986
- The neurofibromatosis‐Noonan syndromeAmerican Journal of Medical Genetics, 1985
- Noonan phenotype associated with neurofibromatosisAmerican Journal of Medical Genetics, 1985
- The neurofibromatosis‐Noonan syndromeAmerican Journal of Medical Genetics, 1985
- A distinctive facial appearance in neurofibromatosis von recklinghausenAmerican Journal of Medical Genetics, 1985