Andersen-Tawil syndrome physical examination
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Charmaine Patel, M.D. [2]; Raviteja Guddeti, M.B.B.S. [3]
Overview
Patients with Andersen-Tawil syndrome usually appear normal. Physical examination of patients with Andersen-Tawil syndrome is usually remarkable for hypoplastic mandible, micrognathia, broad nose , low set ears and clinodactyly.
Physical Examination
Appearance of the Patient
- Patients with Andersen-Tawil syndrome usually appear normal
Head
Findings may include:
- Hypoplastic mandible
- Micrognathia
Eyes
- Hypertelorism may be noted on physical examination
Heart
- Palpitations.
- Syncope usally seen in first or second decade of the life of the patient
- Andersen-Tawil syndrome patients have a unique cardiac findings on ECG
Nose
- Broad nose may be seen
Ears
- Low set ears may be present
Neuromuscular
- Periodic paralysis:
- The most important clinical manifestation of Andersen-Tawil syndrome patients
- Periodic paralysis are episodic paralysis with flaccid muscle weakness
- Muscle weakness:
- In patients with Andersen-Tawil syndrome the muscle weakness occurs intermittently or spontaneously
- Muscle weakness in patients with Andersen-Tawil syndrome may be occured due to prolonged rest or rest following exertion
- Neuromuscular examination of patients with [disease name] is usually normal.
OR
- Patient is usually oriented to persons, place, and time
- Altered mental status
- Glasgow coma scale is ___ / 15
- Clonus may be present
- Hyperreflexia / hyporeflexia / areflexia
- Positive (abnormal) Babinski / plantar reflex unilaterally/bilaterally
- Muscle rigidity
- Proximal/distal muscle weakness unilaterally/bilaterally
- ____ (finding) suggestive of cranial nerve ___ (roman numerical) deficit (e.g. Dilated pupils suggestive of CN III deficit)
- Unilateral/bilateral upper/lower extremity weakness
Extremities
- Periodic paralysis
- Clinodactyly may be present.