Results 121 to 130 of about 1,482 (169)
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Tumefazione sanguinante del palato
Dental Cadmos, 2011Maddalena Manfredi +2 more
exaly +2 more sources
Archives of Otolaryngology - Head and Neck Surgery, 1970
An unusual case of long-standing pseudomembranous inflammation resulted in complete palatalpharyngeal fusion. Extensive studies for diphtheria, fungi, tuberculosis, carcinoma, pemphigus, and upper respiratory scleroma failed to identify the cause.
A S, Miller, R D, Harwick, P A, Pullon
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An unusual case of long-standing pseudomembranous inflammation resulted in complete palatalpharyngeal fusion. Extensive studies for diphtheria, fungi, tuberculosis, carcinoma, pemphigus, and upper respiratory scleroma failed to identify the cause.
A S, Miller, R D, Harwick, P A, Pullon
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Ulcerazione cronica del palato
Dental Cadmos, 2015G Mergoni, L Corcione, I Giovannacci
exaly +4 more sources
The Indian Journal of Pediatrics, 1970
A female child showed features of deafness, characteristic facies and a generalized bone dysplasia, and was diagnosed to have the “oto-palatal-digital syndrome”. The literature is briefly reviewed.
S D, Singh, M S, Diwedi, M, Irani
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A female child showed features of deafness, characteristic facies and a generalized bone dysplasia, and was diagnosed to have the “oto-palatal-digital syndrome”. The literature is briefly reviewed.
S D, Singh, M S, Diwedi, M, Irani
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The oto-palato-digital syndrome
The Journal of Laryngology & Otology, 1976A boy aged ten years with oto-palato-digital syndrome is discussed. Because of severe conductive hearing loss tympanotomy was performed and abnormal poorly mobile ossicles were found. Stapedectomy was performed without improvement of hearing.
L, Podoshin, H S, Heymans, M, Fradis
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Archives of Pediatrics & Adolescent Medicine, 1967
To the Editor .—With regard to our paper (Amer J Dis Child113:214-221, 1967), entitled "Oto-Palato-Digital Syndrome" we have seen another case in a boy who also had identical facies and in the Journal of Medical Genetics 3:17-22, 1966, there appeared to be four other cases reported in boys. This would clearly indicate that this syndrome is inherited as
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To the Editor .—With regard to our paper (Amer J Dis Child113:214-221, 1967), entitled "Oto-Palato-Digital Syndrome" we have seen another case in a boy who also had identical facies and in the Journal of Medical Genetics 3:17-22, 1966, there appeared to be four other cases reported in boys. This would clearly indicate that this syndrome is inherited as
openaire +2 more sources
INHERITANCE OF THE OTO-PALATO-DIGITAL SYNDROME
Archives of Pediatrics & Adolescent Medicine, 1970To the Editor .—Dudding et al 1 in 1967 reported a family with multiple defects and suggested it be called the oto-palato-digital syndrome. In the sibship described there were three affected male subjects. It was suggested that the entity was probably autosomal recessive but could be X-linked.
G, Turner, R J, Gorlin
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The Oto-palato-digital (OPD) Syndrome
Archives of Otolaryngology - Head and Neck Surgery, 1967TAYBI described a case of "generalized skeletal dysplasia with multiple anomalies" in 1962 which did not fit any previously described disease complex. 1 This paper will present three male siblings seen at the University of Minnesota Hospitals with the same spectrum of anomalies.
D J, Buran, A J, Duvall
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Palato-ocular Synchrony During Eyelid Closure
Archives of Neurology, 1976The effects of eyelid closure on oculomotor function was examined in 11 patients with palatal myoclonus. In eight patients, eyelid closure induced gross rhythmic vertical or almost oscillatory movements of the globes, which were synchronous with the rhythmic beat of the palatal myoclonus. The rhythmic vertical ocular movements induced by eyelid closure
L, Jacobs, M B, Bender
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