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1.
Cureus ; 15(9): e45089, 2023 Sep.
Article in English | MEDLINE | ID: mdl-37842451

ABSTRACT

Necrotizing enterocolitis (NEC) following postoperative stress is a rare but life-threatening condition in infants. We report a 3-month-old infant who underwent bilateral inguinal hernia repair and developed NEC. This is the first reported case of an infant developing recurrent NEC with stricture formation after herniotomy. Timely recognition and management are vital due to potentially high mortality rates in severe cases. High index of suspicion is crucial for accurate diagnosis and appropriate management.

2.
Case Rep Pediatr ; 2018: 1543934, 2018.
Article in English | MEDLINE | ID: mdl-30009072

ABSTRACT

Stenotrophomonas maltophilia is an environmental bacterium of growing concern due to its multidrug resistance and pathogenic potential. It is considered an opportunistic pathogen of nosocomial origin most of the time, targeting a specific patients' population. We describe a case of a previously healthy full-term neonate who was found to have S. maltophilia meningitis and was successfully treated with a combination of Trimethoprim-Sulfamethoxazole and Ciprofloxacin.

3.
Am J Med Genet A ; 170A(5): 1142-7, 2016 May.
Article in English | MEDLINE | ID: mdl-26842963

ABSTRACT

ADAT3-related intellectual disability has been recently described in 24 individuals from eight Saudi families who had cognitive impairment and strabismus. Other common features included growth failure, microcephaly, tone abnormalities, epilepsy, and nonspecific brain abnormalities. A single homozygous founder mutation (c.382G>A:p.(V128M)) in the ADAT3 gene, which encodes a protein that functions in tRNA editing, was identified in all affected individuals. In this report, we present additional 15 individuals from 11 families (10 Saudis and 1 Emirati) who are homozygous for the same founder mutation. In addition to the universal findings of intellectual disability and strabismus, the majority exhibited microcephaly and growth failure. Additional features not reported in the original cohort include dysmorphic facial features (prominent forehead, up-slanted palpebral fissures, epicanthus, and depressed nasal bridge), behavioral problems (hyperactivity and aggressiveness), recurrent otitis media, and growth hormone deficiency. ADAT3-related intellectual disability is an important recognizable cause of intellectual disability in Arabia.


Subject(s)
Adenosine Deaminase/genetics , Cognitive Dysfunction/genetics , Intellectual Disability/genetics , Strabismus/genetics , Adolescent , Adult , Child , Child, Preschool , Cognitive Dysfunction/complications , Cognitive Dysfunction/physiopathology , Female , Founder Effect , Growth Hormone/genetics , Humans , Infant , Intellectual Disability/complications , Intellectual Disability/physiopathology , Male , Phenotype , Strabismus/complications , Strabismus/physiopathology
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