Angelo M., mid-20th-century U.S. pediatrician. See: DiGeorge syndrome.
References in periodicals archive ?
Type B IAA is strongly associated with DiGeorge syndrome and chromosome 22q11.
The 22-year-old has learning disabilities, due to a genetic condition called DiGeorge Syndrome, and is also mildly autistic.
His client has autism, ADHD and a chromosomal disorder called DiGeorge syndrome.
Danielle campaigned to raise awareness of DiGeorge syndrome - the rare illness which battered her immune system throughout her life.
6,7) Isolated clinical comorbidities * Laryngomalacia * Subglottic stenosis * Subdural hematoma * Central nervous system malformations including Arnold Chiari malformation * Arthrogryposis * Facial dysmorphic features * Velopharyngeal insufficiency * Hypotonia/myopathy * Ear deformities/sensorineural hearing loss Syndromic associations * Robinow syndrome * Goldenhar syndrome * Down syndrome * Williams syndrome * DiGeorge syndrome * Mobius syndrome * Charcot-Marie-Tooth disease (type 1, 1b and 2) * JS-X syndrome * Hereditary neuralgic amyotrophy * Congenital myasthenic syndrome
1] ARSCA was more common in female than in male and commonly seen in disorders such as Down syndrome, DiGeorge and Edward's syndromes, tetralogy of Fallot, pulmonary atresia, or major aorticopulmonary collateral arteries.
The implication of LZTR1 in human disease was first reported with the DiGeorge Syndrome, as it was deleted in the majority of DiGeorge Syndrome patients [13].
Michael DiGeorge, Vice President of Commercial Aviation and Network Services at Rockwell Collins, said, The advent of the next generation connected cockpit brings with it a new set of requirements in terms of service reliability, availability and security for aviation communications.
Disruption of CXCR4 signaling in pharyngeal neural crest causes DiGeorge syndrome-like malformations.
Liam, a pupil at Heronsbridge School in Bridgend, was born with a genetic condition called DiGeorge syndrome, which had left him with two holes in his heart and valve problems.
7%); autoimmune lymphoproliferative syndrome (10%); lipopolysaccharide-responsive beige-like anchor protein deficiency (10%); and DiGeorge syndrome (10%).
2) These include, among others, the DiGeorge anomaly, Charge syndrome, ataxia telangiectasia, trisomies 18 and 21, and many other genetic syndromes with impaired T cell development.