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1.
Am J Med Genet A ; : e63836, 2024 Aug 16.
Artigo em Inglês | MEDLINE | ID: mdl-39149840

RESUMO

Holoprosencephaly (HPE) results from a lack of cleavage of the prosencephalon. It has a complex etiology, resulting from chromosome abnormalities or single gene variants in the Sonic hedgehog signaling pathway. A single variant, p.Arg535Cys in CNOT1, has been described in HPE in association with pancreatic agenesis and neonatal diabetes. Here, we report on a case of HPE and p.Arg535Cys in CNOT1 without pancreatic agenesis where the patient presented with diabetes mellitus in adolescence. This case reinforces the role of CNOT1 in pancreatic development. We suggest that individuals with p.Arg535Cys in CNOT1 with no pancreas abnormalities observed at birth should be screened for diabetes during follow-up.

2.
Blood ; 118(18): 4957-62, 2011 Nov 03.
Artigo em Inglês | MEDLINE | ID: mdl-21890643

RESUMO

WHIM syndrome is a rare congenital immunodeficiency disorder characterized by warts, hypogammaglobulinemia, infections, and myelokathexis (neutropenia because of impaired egress from the BM); most patients also have severe panleukopenia. Because WHIM syndrome is caused by mutations in the chemokine receptor CXCR4 that result in increased agonist-dependent signaling, we hypothesized that the CXCR4 antagonist plerixafor (Mozobil [Genyzme Corporation], AMD3100), might be an effective treatment. To test this, we enrolled 3 unrelated adult patients with the most common WHIM mutation, CXCR4(R334X), in a phase 1 dose-escalation study. Plerixafor increased absolute lymphocyte, monocyte, and neutrophil counts in blood to normal without significant side effects in all 3 patients. Peak responses occurred at 3-12 hours after injection and waned by 24 hours after injection which tracked the drug's pharmacokinetics. All 3 cell types increased in a dose-dependent manner with the rank order of responsiveness absolute lymphocyte > monocyte > neutrophil. These data provide the first pharmacologic evidence that panleukopenia in WHIM syndrome is caused by CXCL12-CXCR4 signaling-dependent leukocyte sequestration, and support continued study of plerixafor as mechanism-based therapy in this disease. This study is registered at http://www.clinicaltrials.gov as NCT00967785.


Assuntos
Compostos Heterocíclicos/uso terapêutico , Síndromes de Imunodeficiência/tratamento farmacológico , Linfopenia/tratamento farmacológico , Verrugas/tratamento farmacológico , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Fármacos Anti-HIV/administração & dosagem , Fármacos Anti-HIV/farmacocinética , Fármacos Anti-HIV/farmacologia , Fármacos Anti-HIV/uso terapêutico , Benzilaminas , Contagem de Células Sanguíneas , Ciclamos , Relação Dose-Resposta a Droga , Feminino , Compostos Heterocíclicos/administração & dosagem , Compostos Heterocíclicos/farmacocinética , Compostos Heterocíclicos/farmacologia , Humanos , Síndromes de Imunodeficiência/sangue , Síndromes de Imunodeficiência/complicações , Síndromes de Imunodeficiência/genética , Leucócitos/efeitos dos fármacos , Leucócitos/patologia , Linfopenia/complicações , Linfopenia/patologia , Masculino , Pessoa de Meia-Idade , Doenças da Imunodeficiência Primária , Receptores CXCR4/antagonistas & inibidores , Receptores CXCR4/genética , Resultado do Tratamento , Verrugas/sangue , Verrugas/complicações , Verrugas/genética , Adulto Jovem
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