Clinical and electrophysiological studies in a patient with keratitis, ichthyosis and deafness (KID) syndrome
Author:
Publisher
Informa UK Limited
Subject
Cellular and Molecular Neuroscience,Genetics
Link
http://www.tandfonline.com/doi/pdf/10.3109/01677068709102333
Reference15 articles.
1. ATYPICAL ERYTHROKERATODERMA WITH DEAFNESS, PHYSICAL RETARDATION AND PERIPHERAL NEUROPATHY
2. A clinical and electrophysiological study of patients with polychlorinated biphenyl poisoning.
3. Dwarfism with Retinal Atrophy and Deafness
4. A Congenital Ichthyosiform Syndrome With Deafness and Keratitis
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1. Dental Treatments under the General Anesthesia in a Child with Keratitis, Ichthyosis, and Deafness Syndrome;Case Reports in Dentistry;2013
2. Keratitis, Ichthyosis, and Deafness (KID Syndrome): Review of the Literature and Proposal of a New Terminology;Pediatric Dermatology;2010-07-23
3. Dandy-Walker malformation in patients with KID syndrome associated with a heterozygote mutation (p.Asp50Asn) in theGJB2gene encoding connexin 26;Clinical Genetics;2009-10
4. The KID-syndrome in Finland A report of four cases;Acta Ophthalmologica;2009-05-27
5. Successful cochlear implantation in a child with Keratosis, Icthiosis and Deafness (KID) Syndrome and Dandy-Walker malformation;International Journal of Pediatric Otorhinolaryngology;2008-05
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