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1.
Pediatr Dermatol ; 38(5): 1379-1381, 2021 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-34514629

RESUMO

Few cases of pediatric psoriasis with short stature, possibly resulting from chronic systemic inflammation, have been reported. We present the case of a child with short stature occurring after the onset of psoriasis wherein treatment with adalimumab resulted in the improvement of not only the psoriasis but also the child's short stature. Pediatric psoriasis associated with short stature may benefit from the early induction of biologic therapy.


Assuntos
Nanismo , Psoríase , Adalimumab/efeitos adversos , Anticorpos Monoclonais , Terapia Biológica , Criança , Humanos , Psoríase/tratamento farmacológico
2.
Eur J Med Genet ; 61(10): 631-633, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29673649

RESUMO

22q13 deletion syndrome is a genetic disorder caused by the deletion or disruption of the segment of the long arm of chromosome 22. The characteristic clinical features of this syndrome include delayed expressive speech, autistic behavior and hypotonia, and clinically severe complications associated with autoimmunity are rarely reported. We herein report a girl with 22q13 deletion syndrome complicated with multiple inflammatory and autoimmune diseases during early childhood. We performed whole-exome sequencing to identify the genes responsible for her autoimmune diseases and identified the de novo variant p.R512W in the phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta (PIK3CD) gene. We suspected it to be the disease-causing variant at the conserved residue in PIK(3)C p110δ. Alternatively, haplo-insufficiency of SHANK3 or other genes by 22q13 deletion and the PIK3CD variant might have synergistically contributed to the onset of the distinctive clinical manifestations in this patient.


Assuntos
Doenças Autoimunes/genética , Transtornos Cromossômicos/genética , Classe I de Fosfatidilinositol 3-Quinases/genética , Doenças Autoimunes/diagnóstico , Deleção Cromossômica , Transtornos Cromossômicos/diagnóstico , Transtornos Cromossômicos/imunologia , Cromossomos Humanos Par 22/genética , Cromossomos Humanos Par 22/imunologia , Feminino , Humanos , Lactente , Mutação
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