Familial hemicrania continua

Author:

Weatherall Mark W1,Bahra Anish2

Affiliation:

1. Charing Cross Hospital, UK.

2. National Hospital for Neurology and Neurosurgery, UK.

Abstract

There are now three known causative genes for familial hemiplegic migraine and increasing evidence to support a genetic predisposition to the more common types of migraine with and without aura, and for cluster headache. We present the first reported case of familial hemicrania continua. A mother and daughter developed hemicrania continua at the same time of life. Both showed an absolute response to indometacin and at similar doses. Both also suffered from migraine with aura. We discuss the increasing support for a genetic predisposition to dysfunction of the pain system within the brain manifesting as primary headache.

Publisher

SAGE Publications

Subject

Neurology (clinical),General Medicine

Cited by 15 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Paroxysmal hemicrania and hemicrania continua: Review on pathophysiology, clinical features and treatment;Cephalalgia;2023-11

2. Hemicrania continua in a family: A report of two cases;Headache: The Journal of Head and Face Pain;2021-07

3. Hemicrania Continua: An Update;Neurology India;2021

4. Cluster headache and TACs: state of the art;Neurological Sciences;2020-08-26

5. Genetics of Cluster Headache and Other Trigeminal Autonomic Cephalalgias;Cluster Headache and other Trigeminal Autonomic Cephalgias;2019-07-18

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