Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
1.
Brain Dev ; 44(10): 732-736, 2022 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-35907674

RESUMEN

INTRODUCTION: Congenital disorders of glycosylation (CDG) are inherited inborn errors of metabolism due to abnormal protein and lipid glycosylation that present with multi-systemic manifestations. The heterogeneity of CDG poses a serious diagnostic challenge; therefore, whole-exome sequencing (WES), which plays an increasingly important role in the molecular diagnosis of CDG, is used for examining patients with CDG. CASE REPORT: We report the case of a two-month-old male patient who developed developmental and epileptic encephalopathy (DEE) with intractable seizures and microcephaly. EEG demonstrated a suppression-burst (S-B) pattern, and MRI showed delayed myelination and progressive atrophic changes. Although CDG was clinically suspected, serum transferrin isoelectric focusing analysis appeared to be normal. The patient died by six years of age. Postmortem WES performed approximately 20 years after the patient's death revealed homozygous variants in ALG11 (NM_001004127.3: c.935A > C, p.Glu312Ala), and the patient was diagnosed with ALG11-CDG. CONCLUSION: We present a case of the patient with ALG11-CDG diagnosed using post-mortem WES. The EEG revealed a S-B pattern that indicated severely drug-resistant DEE, which was associated with poor prognosis. If a CDG is suspected, WES should be considered.


Asunto(s)
Trastornos Congénitos de Glicosilación , Microcefalia , Humanos , Masculino , Lactante , Trastornos Congénitos de Glicosilación/diagnóstico , Trastornos Congénitos de Glicosilación/genética , Secuenciación del Exoma , Glicosilación , Homocigoto , Transferrina/metabolismo , Manosiltransferasas/genética
2.
No To Hattatsu ; 38(6): 419-24, 2006 Nov.
Artículo en Japonés | MEDLINE | ID: mdl-17094560

RESUMEN

We report 10 cases of pulmonary atelectasis diagnosed by chest computed tomography in patients with neurological or muscular disease. Atelectasis was frequently seen in hypotonic patients who could not roll over on their own. The atelectases located mostly in the dorsal bronchopulmonary segments, adjacent to the heart or diaphragm. Atelectasis diminished in two patients after they became able to roll themselves over. Gravity-related lung compression by the heart and intra-abdominal organs on persistent supine position can cause pulmonary atelectasis in patients with neurological or muscular disease who can not roll over by their own power. To confirm that the prone position reduces compression of the lungs, chest computed tomography was performed in both the supine and the prone position in three patients. Sagittal images with three-dimensional computed tomographic reconstruction revealed significant sternad displacements of the heart and caudal displacements of the dorsal portion of the diaphragm on prone position compared with supine position. The prone position, motor exercises for rolling over, and biphasic cuirass ventilation are effective in reducing gravity-related lung compression. Some patients with intellectual disabilities were also able to cooperate in chest physiotherapy. Chest physiotherapy is useful in preventing atelectasis in patients with neurological or muscular disease.


Asunto(s)
Gravitación , Pulmón/fisiopatología , Enfermedades Musculares/complicaciones , Enfermedades del Sistema Nervioso/complicaciones , Atelectasia Pulmonar/fisiopatología , Posición Supina , Abdomen/fisiopatología , Adolescente , Niño , Preescolar , Femenino , Corazón/fisiopatología , Humanos , Lactante , Masculino , Respiración con Presión Positiva , Presión/efectos adversos , Atelectasia Pulmonar/etiología , Atelectasia Pulmonar/terapia
3.
No To Hattatsu ; 38(3): 177-81, 2006 May.
Artículo en Japonés | MEDLINE | ID: mdl-16715930

RESUMEN

The purpose of this study is to clear up the difference between Asperger's disorder (AS) and high functioning autism (HFA) with a newly developed test, the metaphor and sarcasm scenario test (MSST) can be used to distinguish pervasive developmental disorder (PDD) from attention deficit/hyperactivity disorders (AD/HD). So 66 AS children, 20 HFA children and 37 AD/HD children were selected, compared the profiles of score on the MSST. The results showed that the inability to understand sarcastic situation was specific to group with AS, both group with HFA and AD/HD were differ little to understand between metaphor and sarcasm. In this study suggest differences in situational recognition among the PDD subtypes, the clinical symptoms of PDD reflects characteristics of AS.


Asunto(s)
Síndrome de Asperger/diagnóstico , Trastorno por Déficit de Atención con Hiperactividad/diagnóstico , Trastorno Autístico/diagnóstico , Pruebas Neuropsicológicas , Pruebas Psicológicas , Reconocimiento en Psicología , Adolescente , Síndrome de Asperger/psicología , Trastorno por Déficit de Atención con Hiperactividad/psicología , Trastorno Autístico/psicología , Niño , Femenino , Humanos , Masculino , Desempeño Psicomotor/fisiología , Percepción Social
4.
Brain Dev ; 26(5): 301-6, 2004 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-15165670

RESUMEN

It is sometimes difficult to discriminate high functioning pervasive developmental disorders (HFPDD) from attention deficit/hyperactivity disorders (AD/HD) in young children because of the behavioral similarities between the two. For adequate diagnosis, understanding fundamental differences in their social cognitive abilities might become significant. In order to detect the differences in social cognitive abilities between AD/HD and HFPDD, a new test, the Metaphor and Sarcasm Scenario Test (MSST) was developed. One hundred and ninety-nine normal school children (the control group), 29 AD/HD children and 54 HFPDD children were involved. The results showed that the inability to understand a sarcastic situation was specific to children with HFPDD, both children with AD/HD and HFPDD could not equally understand metaphor. The correlation between the comprehension of sarcasm and success in the theory of mind task was remarkably high but not for comprehension of metaphor. In conclusion, the MSST has the potential to discriminate HFPDD from AD/HD in young children.


Asunto(s)
Trastorno por Déficit de Atención con Hiperactividad/diagnóstico , Trastorno por Déficit de Atención con Hiperactividad/psicología , Discapacidades del Desarrollo/diagnóstico , Discapacidades del Desarrollo/psicología , Pruebas Neuropsicológicas , Percepción Social , Niño , Diagnóstico Diferencial , Femenino , Humanos , Masculino , Desempeño Psicomotor/fisiología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA