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Cognitive and behavioral phenotype of children with pseudohypoparathyroidism type 1A.
Perez, Katia M; Lee, Evon B; Kahanda, Sachini; Duis, Jessica; Reyes, Monica; Jüppner, Harald; Shoemaker, Ashley H.
Afiliação
  • Perez KM; Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Lee EB; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Kahanda S; Division of Pediatric Endocrinology, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Duis J; Department of Pediatrics, Division of Medical Genetics and Genomic Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Reyes M; Endocrine Unit and Pediatric Nephrology Unit, Massachusetts General Hospital and Harvard Medical School Boston, Boston, Massachusetts.
  • Jüppner H; Endocrine Unit and Pediatric Nephrology Unit, Massachusetts General Hospital and Harvard Medical School Boston, Boston, Massachusetts.
  • Shoemaker AH; Division of Pediatric Endocrinology, Vanderbilt University Medical Center, Nashville, Tennessee.
Am J Med Genet A ; 176(2): 283-289, 2018 02.
Article em En | MEDLINE | ID: mdl-29193623
ABSTRACT
Pseudohypoparathyroidism 1A (PHP1A) is a rare, genetic disorder. Most patients with PHP1A have cognitive impairment but this has not been systematically studied. We hypothesized that children with PHP1A would have lower intelligent quotient (IQ) scores than controls. To evaluate cognition and behavior, we prospectively enrolled children with PHP1A, one unaffected sibling (when available) and controls matched on BMI/age/gender/race. Evaluations included cognitive and executive function testing. Parents completed questionnaires on behavior and executive function. We enrolled 16 patients with PHP1A, 8 unaffected siblings, and 15 controls. Results are presented as mean (SD). The PHP1A group had a composite IQ of 85.9 (17.2); 25% had a composite IQ < -2 SD. The PHP1A group had significantly lower IQs than matched controls (composite IQ -17.3, 95%CI -28.1 to -6.5, p < 0.01) and unaffected siblings (composite IQ -21.5, 95%CI -33.9 to -9.1, p < 0.01). Special education services were utilized for 93% of the patients with PHP1A. Deficits were observed in executive function and parents reported delayed adaptive behavior skills and increased rates of attention deficit hyperactivity disorder. In conclusion, children with PHP1A have lower intelligence quotient scores, poorer executive function, delayed adaptive behavior skills, and increased behavior problems.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Pseudo-Hipoparatireoidismo / Comportamento Infantil / Cognição Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Qualitative_research / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Pseudo-Hipoparatireoidismo / Comportamento Infantil / Cognição Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Qualitative_research / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article