82 top medical experts on Opitz-Kaveggia syndrome across 6 countries and 4 U.S. states, including 7 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Opitz-Kaveggia syndrome: A rare X-linked syndromic intellectual disability characterized by developmental delay and intellectual disability, early hypotonia, constipation, feeding problems, imperforate anus, characteristic behavior (affable, eager to please), and dysmorphic craniofacial features (such as relative macrocephaly, prominent forehead with frontal hair upsweep, hypertelorism, downslanting palpebral fissures, and open mouth). Additional manifestations are partial agenesis of the corpus callosum, sensorineural hearing loss, joint laxity, cardiac anomalies, and abnormalities of the fingers and toes, among others.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Support Organizations
- National Organization of Disorders of the Corpus Callosum
PMB 363
18032-C Lemon Drive
Yorba Linda, CA 92886
Telephone: +1-714-747-0063
Fax: +1-714-693-0808
E-mail: info@nodcc.org
Website: https://nodcc.org/
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- Synonyms: FG syndrome, FG syndrome 1, FG syndrome 2, FG syndrome 3, FG syndrome 4, FGS1, Keller syndrome, and Partial Agenesis of the Corpus Callosum Congenital Hypotonia Imperforate Anus Large Head Mental Retardation, Cask-Related X-Linked Mental Retardation, With Nystagmus X-Linked Mental Retardation
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