Add to ORKGWe describe a family in whom a pericentric inversion of chromosome 5 segregates with benign familial neonatal convulsions (BFNC). BFNC is an autosomal dominant form of epilepsy characterised by spontaneous partial or generalised clonic convulsions beginning within the first months of life. Seizures usually disappear by the age of 6 months; intercritical electroencephalogram and subsequent psychomotor development are normal. BFNC loci have been mapped to human chromosomes 20q13.3 (BFNC1) and 8q24 (BFNC2), based on linkage analysis
We present a patient (3 months old) with partial and generalized seizures who has a family history o...
SummaryBenign infantile familial convulsions is an autosomal dominant disorder characterized by nonf...
Over the past decade and a half, considerable advances have been made in the understanding of the mo...
We describe a family in whom a pericentric inversion of chromosome 5 segregates with benign familial...
Two autosomal dominant forms of benign idiopathic epilepsy of early life have been described: benign...
Purpose: Benign familial infantile convulsions (BFIC) is a form of idiopathic epilepsy. It is charac...
Benign familial infantile convulsions (BFIC) are an autosomal-dominant epileptic syndrome characteri...
Linkage studies with the chromosome 20 markers D20S19 and D20S20 were performed in two families with...
Benign familial infantile convulsions (BFIC) is an autosomal dominantly inherited partial epilepsy s...
The syndrome of benign familial infantile convulsions (BFIC) is an autosomal dominant epileptic diso...
The syndrome of benign familial infantile convulsions (BFIC) is an autosomal dominant epileptic diso...
Benign infantile familial convulsions is an autosomal dominant disorder characterized by nonfebrile ...
In 1997, a locus for benign familial infantile convulsions (BFIC) was mapped to chromosome 19q. Furt...
Purpose: A locus for benign familial convulsions (BFICs) has been recently mapped on chromosome 19q1...
We present a patient (3 months old) with partial and generalized seizures who has a family history o...
We present a patient (3 months old) with partial and generalized seizures who has a family history o...
SummaryBenign infantile familial convulsions is an autosomal dominant disorder characterized by nonf...
Over the past decade and a half, considerable advances have been made in the understanding of the mo...
We describe a family in whom a pericentric inversion of chromosome 5 segregates with benign familial...
Two autosomal dominant forms of benign idiopathic epilepsy of early life have been described: benign...
Purpose: Benign familial infantile convulsions (BFIC) is a form of idiopathic epilepsy. It is charac...
Benign familial infantile convulsions (BFIC) are an autosomal-dominant epileptic syndrome characteri...
Linkage studies with the chromosome 20 markers D20S19 and D20S20 were performed in two families with...
Benign familial infantile convulsions (BFIC) is an autosomal dominantly inherited partial epilepsy s...
The syndrome of benign familial infantile convulsions (BFIC) is an autosomal dominant epileptic diso...
The syndrome of benign familial infantile convulsions (BFIC) is an autosomal dominant epileptic diso...
Benign infantile familial convulsions is an autosomal dominant disorder characterized by nonfebrile ...
In 1997, a locus for benign familial infantile convulsions (BFIC) was mapped to chromosome 19q. Furt...
Purpose: A locus for benign familial convulsions (BFICs) has been recently mapped on chromosome 19q1...
We present a patient (3 months old) with partial and generalized seizures who has a family history o...
We present a patient (3 months old) with partial and generalized seizures who has a family history o...
SummaryBenign infantile familial convulsions is an autosomal dominant disorder characterized by nonf...
Over the past decade and a half, considerable advances have been made in the understanding of the mo...