Add to ORKGNeurofibromatosis (NF), Noonan syndrome (NS), and LEOPARD syndrome are all autosomal dominant conditions, each being a distinct clinical entity by itself. Rarely, one encounters cases with features of NF and NS and is termed as the 'Neurofibromatosis-Noonan syndrome' (NF-NS). The authors report a clinical dilemma with major clinical features of the NF-NS syndrome and LEOPARD syndrome co-existing in the same patient. Also, features of Noonan syndrome and LEOPARD syndrome are compared with the case reported
Neurofibromatosis type 1 (NF1) is one of the most frequent genetic disorders, affecting 1:3,000 worl...
The L.E.O.P.A.R.D. syndrome is an autosomal, dominant disorder with characteristic features that inc...
LEOPARD syndrome, also known as Gorlin syndrome II, cardiocutaneous syndrome, lentiginosis profusa s...
Neurofibromatosis (NF), Noonan syndrome (NS), and LEOPARD syndrome are all autosomal dominant condit...
Noonan syndrome with multiple lentigines (NSML), formerly known as LEOPARD syndrome, is an autosomal...
Diagnosis within RASopathies still represents a challenge. Nevertheless, many efforts have been mad...
Neurofibromatosis (NF) Type 1 (NF-1) is an autosomal dominant disease with a prevalence of about 1/3...
LEOPARD syndrome is a complex disorder characterized by multiple dysmorphogenetic features. Both syn...
case reportNeurofibromatosis–Noonan syndrome is a rare autosomal dominant disorder which combines ne...
LEOPARD syndrome (LS) is an autosomal dominant syndrome characterized by multiple lentigines and caf...
The association of the Noonan phenotype with neurofibromatosis type 1 (NF1) was first noted by Allan...
Noonan syndrome (NS) is an autosomal dominant disease caused by aberrant up-regulated signaling thro...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Neurofibromatosis?Noonan syndrome (NFNS) is an uncommon chromosomal disorder showing features of bot...
LEOPARD syndrome, also known as Gorlin syndrome II, cardiocutaneous syndrome, lentiginosis profusa s...
Neurofibromatosis type 1 (NF1) is one of the most frequent genetic disorders, affecting 1:3,000 worl...
The L.E.O.P.A.R.D. syndrome is an autosomal, dominant disorder with characteristic features that inc...
LEOPARD syndrome, also known as Gorlin syndrome II, cardiocutaneous syndrome, lentiginosis profusa s...
Neurofibromatosis (NF), Noonan syndrome (NS), and LEOPARD syndrome are all autosomal dominant condit...
Noonan syndrome with multiple lentigines (NSML), formerly known as LEOPARD syndrome, is an autosomal...
Diagnosis within RASopathies still represents a challenge. Nevertheless, many efforts have been mad...
Neurofibromatosis (NF) Type 1 (NF-1) is an autosomal dominant disease with a prevalence of about 1/3...
LEOPARD syndrome is a complex disorder characterized by multiple dysmorphogenetic features. Both syn...
case reportNeurofibromatosis–Noonan syndrome is a rare autosomal dominant disorder which combines ne...
LEOPARD syndrome (LS) is an autosomal dominant syndrome characterized by multiple lentigines and caf...
The association of the Noonan phenotype with neurofibromatosis type 1 (NF1) was first noted by Allan...
Noonan syndrome (NS) is an autosomal dominant disease caused by aberrant up-regulated signaling thro...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Neurofibromatosis?Noonan syndrome (NFNS) is an uncommon chromosomal disorder showing features of bot...
LEOPARD syndrome, also known as Gorlin syndrome II, cardiocutaneous syndrome, lentiginosis profusa s...
Neurofibromatosis type 1 (NF1) is one of the most frequent genetic disorders, affecting 1:3,000 worl...
The L.E.O.P.A.R.D. syndrome is an autosomal, dominant disorder with characteristic features that inc...
LEOPARD syndrome, also known as Gorlin syndrome II, cardiocutaneous syndrome, lentiginosis profusa s...