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H. P. Gibb
British neurologist.
Associated eponyms:
Curschmann-Batten-Steinert Syndrome
Rare hereditary familial disease characterized by progressive muscular wasting, myotonia, cataracts, hypogonadism, and mental deterioration.
Biography:
Bibliography:
- Two cases of myotonia atrophica, showing a peculiar distribution of muscular atrophy.
With Frederick Eustace Batten.
Proceedings of the Royal Society of Medicine, London, Neurol Section, 1908; 32.
- Myotonia atrophica.
With Frederick Eustace Batten. Brain, Oxford, 1909, 32: 187-205.
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