|Signs and Symptoms||Approximate number of patients (when available)|
|Specific learning disability||7.5%|
|Antegonial notching of mandible||-|
|Autosomal dominant inheritance||-|
|Bidirectional ventricular ectopy||-|
|Clinodactyly of the 5th finger||-|
|Clinodactyly of the 5th toe||-|
|Delayed eruption of permanent teeth||-|
|Delayed skeletal maturation||-|
|Hypoplasia of dental enamel||-|
|Hypoplasia of the maxilla||-|
|Periodic hypokalemic paresis||-|
|Persistence of primary teeth||-|
|Prolonged QT interval||-|
|Prominent frontal sinuses||-|
|Short mandibular rami||-|
|Short palpebral fissure||-|
|Short phalanx of finger||-|
|Slender long bone||-|
1. Two of the following three criteria:
2. One of the above three criteria in addition to at least one other family member who meets two of the three criteria.The presence of a mutation in the KCNJ2 gene confirms the diagnosis of Andersen-Tawil syndrome.
The resources below provide information about treatment options for this condition. If you have questions about which treatment is right for you, talk to your healthcare professional.
Research helps us better understand diseases and can lead to advances in diagnosis and treatment. This section provides resources to help you learn about medical research and ways to get involved.
Nonprofit support and advocacy groups bring together patients, families, medical professionals, and researchers. These groups often raise awareness, provide support, and develop patient-centered information. Many are the driving force behind research for better treatments and possible cures. They can direct people to research, resources, and services. Many groups also have experts who serve as medical advisors. Visit their website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD. Suggest an organization to add.