✦ LIBER ✦

Anaesthetic considerations for the patient with cri du chat syndrome

✍ Scribed by ROBERT P. BRISLIN; STEPHEN A. STAYER; ROY E. SCHWARTZ

Book ID: 109029028
Publisher: John Wiley and Sons
Year: 1995
Tongue: English
Weight: 253 KB
Volume: 5
Category: Article
ISSN: 1155-5645
DOI: 10.1111/j.1460-9592.1995.tb00262.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Educational Priorities for Children with

Educational Priorities for Children with Cri-Du-Chat Syndrome

✍ Keenan A. Pituch; Vanessa A. Green; Robert Didden; Lisa Whittle; Mark F. O’Reill 📂 Article 📅 2009 🏛 Springer US 🌐 English ⚖ 189 KB

Screening for minute deletions in patien

Screening for minute deletions in patients with suspected cri-du-chat syndrome and apparently normal karyotype

✍ H. Hoehn; W. Engel 📂 Article 📅 1969 🏛 Springer 🌐 English ⚖ 351 KB

Cri du chat syndrome and complex karyoty

Cri du chat syndrome and complex karyotype in a patient with infantile spasms, hypsarrhythmia, nonketotic hyperglycinemia, and heterotopia

✍ Chang Y. Tsao; Gail D. Wenger; Dennis W. Bartholomew 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 99 KB 👁 2 views

Partial monosomy 22 as the result of an

Partial monosomy 22 as the result of an unbalanced translocation 5:22 in a patient with cri-du-chat syndrome

✍ Margherita Cirillo Silengo; Generoso Andria 📂 Article 📅 1976 🏛 Springer 🌐 English ⚖ 197 KB

A 2-year-old boy with features suggestive of cri-du-chat syndrome had a complex karyotype: 45,XY,--22,5p--,t(5p:22q). Clinical symptoms were catlike cry in early infancy, severe mental and motor retardation, failure to thrive, hypertelorism, antimongoloid slant of the eyes, ptosis of the eyelids, ep

Characterization of a de novo complex ch

Characterization of a de novo complex chromosomal rearrangement in a patient with cri-du-chat and trisomy 5p syndromes

✍ Ascensión Vera-Carbonell; Juan Antonio Bafalliu; Encarna Guillén-Navarro; Ariadn 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 378 KB 👁 2 views

## Abstract Two syndromes with abnormalities of the short arm of chromosome 5 have been described: cri‐du‐chat (resulting from 5p deletion) and trisomy 5p. We report for the first time a patient with both syndromes, resulting from a complex chromosomal rearrangement with an inverted duplication of

Studies of the cranial base in 23 patien

Studies of the cranial base in 23 patients with cri-du-chat syndrome suggest a cranial developmental field involved in the condition

✍ Kj�r, Inger; Niebuhr, Erik 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 82 KB 👁 2 views

The purpose of the present study was to investigate the cranial base on profile radiographs of patients with cri-du-chat syndrome and to relate the findings to current knowledge of brain malformation in an attempt to localize the developmental field affected in cri-du-chat syndrome. The material of