Neurofibromatosis (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?Noonan syndrome (NFNS) is an uncommon chromosomal disorder showing features of bot...
Abstract LEOPARD syndrome (LS, OMIM 151100) is a rare multiple congenital anomalies condition, mainl...
Noonan syndrome (NS) and the clinically overlapping disorders cardio-facio-cutaneous syndrome, LEOPA...
Neurofibromatosis (NF), Noonan syndrome (NS), and LEOPARD syndrome are all autosomal dominant condit...
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...
case reportNeurofibromatosis–Noonan syndrome is a rare autosomal dominant disorder which combines ne...
LEOPARD syndrome is a complex disorder characterized by multiple dysmorphogenetic features. Both syn...
LEOPARD syndrome (LS) is an autosomal dominant syndrome characterized by multiple lentigines and caf...
Neurofibromatosis (NF) Type 1 (NF-1) is an autosomal dominant disease with a prevalence of about 1/3...
The association of the Noonan phenotype with neurofibromatosis type 1 (NF1) was first noted by Allan...
Neurofibromatosis type 1 (NF1) demonstrates phenotypic overlap with Noonan syndrome (NS) in some pat...
Neurofibromatosis type 1 (NF1) demonstrates phenotypic overlap with Noonan syndrome (NS) in some pat...
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...
Abstract LEOPARD syndrome (LS, OMIM 151100) is a rare multiple congenital anomalies condition, mainl...
Noonan syndrome (NS) and the clinically overlapping disorders cardio-facio-cutaneous syndrome, LEOPA...
Neurofibromatosis (NF), Noonan syndrome (NS), and LEOPARD syndrome are all autosomal dominant condit...
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...
case reportNeurofibromatosis–Noonan syndrome is a rare autosomal dominant disorder which combines ne...
LEOPARD syndrome is a complex disorder characterized by multiple dysmorphogenetic features. Both syn...
LEOPARD syndrome (LS) is an autosomal dominant syndrome characterized by multiple lentigines and caf...
Neurofibromatosis (NF) Type 1 (NF-1) is an autosomal dominant disease with a prevalence of about 1/3...
The association of the Noonan phenotype with neurofibromatosis type 1 (NF1) was first noted by Allan...
Neurofibromatosis type 1 (NF1) demonstrates phenotypic overlap with Noonan syndrome (NS) in some pat...
Neurofibromatosis type 1 (NF1) demonstrates phenotypic overlap with Noonan syndrome (NS) in some pat...
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...
Abstract LEOPARD syndrome (LS, OMIM 151100) is a rare multiple congenital anomalies condition, mainl...
Noonan syndrome (NS) and the clinically overlapping disorders cardio-facio-cutaneous syndrome, LEOPA...
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