References
- Tyler F H, Stephens F E. Studies in disorders of muscle. II. Clinical manifestations and inheritance of fa-cioscapulohumeral dystrophy in a large family. Ann Intern Med 1950; 32: 640–60
- Kazakov V M, Bogorodinsky D K, Znoyko Z V, Sko-Rometz A A. The facio-scapulo-limb (or the facioscapu-lohumeral) type of muscular dystrophy. Clinical and genetic study of 200 cases. Eur Neurol 1974; 11: 236–60
- Padberg G. Facioscapulohumeral disease. Thesis, Leiden University. 1982
- Wijmenga C, Frants R R, Brouwer O F, Moerer P, Weber J L, Padberg G W. Location of facioscapulohumeral muscular dystrophy gene on chromosome 4. Lancet. 1990; 336: 651–3
- Toriyama M, Takeuchi M, Kaida T, et al. Hearing impairment in cases of progressive muscle atrophic diseases. Otolaryngology (Tokyo) 1973; 45: 7–16
- Hiraide F, Kodera K, Iinuma T. Sensori-neural deafness in two cases of progressive muscular atrophic disease. Audiol Jpn 1975; 18: 208–13
- Carroll J E, Brook M H. Infantile facioscapulohumeral dystrophy. Peroneal atrophies and related disorders, G Serratrice, H Roux. Masson, New York 1979; 305–19
- Meyerson M D, Lewis E K, III. Facioscapulohumeral muscular dystrophy and accompanying hearing loss. Arch Otolaryngol 1984; 110: 261–6
- Korf B R, Bresnan M J, Shapiro F, Sotrel A, Abroms I F. Facioscapulohumeral dystrophy presenting in infancy with facial diplegia and sensorineural deafness. Ann Neurol 1985; 17: 513–6
- Voit T, Lamprecht A, Lenard H-G, Goebel H H. Hearing loss in facioscapulohumeral dystrophy. Eur J Pedi-atr 1986; 145: 280–5
- Brouwer O F, Padberg G W, Ruys C JM, Brand R, de Laat J APM, Grote J J. Hearing loss in facioscapulohumeral muscular dystrophy. Neurology 1991; 41: 1878–81
- Taylor D A, Carroll J E, Smith M E, Johnson M O, Johnston G P, Brooke M H. Facioscapulohumeral dystrophy asSociated with hearing loss and Coats syndrome. Ann Neurol 1982; 12: 395–8
- Wulff J D, Lin J T, Kepes J J. Inflammatory facioscapulohumeral muscular dystrophy and Coats syndrome. Ann Neurol 1982; 12: 398–401
- Gieron M A, Korthals J K, Kousseff B G. Facioscapulohumeral dystrophy with cochlear hearing loss and tortuosity of retinal vessels. Am J Med Genet 1985; 22: 143–7
- Gurwin E B, Fitzsimons R B, Sehmi K S, Bird A C. Retinal telangiectasis in facioscapulohumeral muscular dystrophy with deafness. Arch Opthalmol 1985; 103: 1695–700
- Yasukohchi S, Yagi Y, Akabane T, Terauchi A, Tama-Gawa K, Mizuno Y. Facioscapulohumeral dystrophy associated with sensorineural hearing loss, tortuosity of retinal arterioles, and an early onset and rapid progression of respiratory failure. Brain Dev 1988; 10: 319–24
- Small R G. Coats' disease and muscular dystrophy. Trans Am Acad Ophthalmol Otolaryngol 1968; 72: 225–31
- Matsuzaka T, Sakuragawa N, Terasawa K, Kuwabara H. Facioscapulo-humeral dystrophy associated with mental retardation, hearing loss, and tortuosity of retinal arterioles. J Child Neurol 1986; 1: 218–23
- Verhagen W IM, Ter Bruggen J P, Huygen P LM. Oculomotor, auditory, and vestibular responses in myotonic dystrophy. Arch Neurol 1992; 49: 954–60
- Wijmenga C, Padberg G W, Moerer P, et al. Mapping of facioscapulohumeral muscular dystrophy gene on chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization. Genomics 1991; 9: 570–5
- Wijmenga C, Hewitt J E, Sandkuijl L, et al. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy. Nature Genetics 1992; 2: 26–30
- Wijmenga C, Brouwer O F, Padberg G W, Frants R R. Transmission of denovo mutation asSociated with facioscapulohumeral muscular dystrophy. Lancet 1992; 340: 984–5
- Theunissen E JJM, Huygen P LM, Folgering H T. Vestibular hyperreactivity and hyperventilation. Clin Otolaryngol 1986; 11: 161–9
- Nijhuis B G, Huygen P LM. Single-response variability of air and water caloric reactions. ORL J Otorhinolar-yngol Relat Spec 1980; 42: 196–205
- Brouwer O F, Wijmenga C, Frants R R, Padberg G W. Fascioscapulo-humeral muscular dystrophy: the impact of genetic research (review). Clin Neurol Neurosurg 1993; 95: 9–21