ROYER SYNDROMES
\ɹˈɔ͡ɪə sˈɪndɹə͡ʊmz], \ɹˈɔɪə sˈɪndɹəʊmz], \ɹ_ˈɔɪ_ə s_ˈɪ_n_d_ɹ_əʊ_m_z]\
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A chromosomal disorder associated with a deletion of the proximal portion of the long arm of chromosome 15 (15q11-q13) in the majority of affected individuals. The abnormalities occur exclusively on the paternally derived chromosome 15. Clinical manifestations include MENTAL RETARDATION, muscular hypotonia, OBESITY, hyperphagia, short stature, hypogonadism, strabismus, and hypersomnolence. (Menkes, Textbook of Child Neurology, 5th ed, p229)
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Platidiam
- An inorganic water-soluble platinum complex. After undergoing hydrolysis, it reacts DNA produce both intra interstrand crosslinks. These crosslinks appear to impair replication and transcription of DNA. The cytotoxicity cisplatin correlates with cellular arrest in G2 phase cell cycle.
Nearby Words
- royalties
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- royer syndrome
- Royer Syndromes
- royers syndrome
- royne
- roynish
- royster
- roysterer