A boy with developmental regression
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چکیده
منابع مشابه
CHALLENGING CASE: DEVELOPMENTAL DELAYS AND REGRESSIONS A Two-Year-Old Boy with Language Regression and Unusual Social Interactions*
CASE Jimmy, a 21⁄2-year-old boy, was seen for the first time by a new pediatrician after a recent family move. His mother made the appointment for a health supervision visit although she had concerns about his language and social skills. She stated that he spoke primarily with unintelligible sounds and often communicated by pointing with his finger. He spoke only 10 words that were clear enough...
متن کاملCHALLENGING CASE: DEVELOPMENTAL DELAYS AND REGRESSIONS A Two-Year-Old Boy with Language Regression and Unusual Social Interactions*
CASE Jimmy, a 21⁄2-year-old boy, was seen for the first time by a new pediatrician after a recent family move. His mother made the appointment for a health supervision visit although she had concerns about his language and social skills. She stated that he spoke primarily with unintelligible sounds and often communicated by pointing with his finger. He spoke only 10 words that were clear enough...
متن کاملDevelopmental regression and irritability
Submitted by: Naif M. AlAnazy, MD, Saad A. Al-Shahwan, MD, Zeeshan Azmat, MD, Brahim Tabarki, MD. From the Division of Pediatric Neurology (AlAnazy, Al-Shahwan, Tabarki), Department of Pediatrics, and the Division of Neuroradiology (Azmat), Department of Radiology, Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia. Address correspondence to: Dr. Brahim Tabarki, Division of Ne...
متن کاملA boy with developmental delay and a maternally inherited deletion in 15q11q13.
A boy was referred at 8 weeks of age for failure to thrive. Cytogenetic and molecular studies showed that he had a large proximal deletion of the maternally derived chromosome 15q. He did not have Angelman syndrome, but at 2 years of age was severely globally delayed. He died at 2 1/2 years of age.
متن کاملMultiple congenital anomalies and developmental delay in a boy associated with a de novo 16p13.3 deletion.
We describe a patient with multiple congenital anomalies including tracheobronchomalacia, CT-proven metopic craniosynostosis, glandular hypospadias and severe ventral chordee, torticollis, esotropia, strabismus, fifth finger clinodactyly, hallux valgus, and global developmental delay. Using high resolution chromosomal microarray analysis, we identified a de novo deletion of 555 kb on chromosome...
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ژورنال
عنوان ژورنال: Paediatrics & Child Health
سال: 2018
ISSN: 1205-7088,1918-1485
DOI: 10.1093/pch/pxy067