Indonesian
Albanian
Arabic
Armenian
Azerbaijani
Belarusian
Bengali
Bosnian
Catalan
Czech
Danish
Deutsch
Dutch
English
Estonian
Finnish
Français
Greek
Haitian Creole
Hebrew
Hindi
Hungarian
Icelandic
Indonesian
Irish
Italian
Japanese
Korean
Latvian
Lithuanian
Macedonian
Mongolian
Norwegian
Persian
Polish
Portuguese
Romanian
Russian
Serbian
Slovak
Slovenian
Spanish
Swahili
Swedish
Turkish
Ukrainian
Vietnamese
Български
中文(简体)
中文(繁體)
hyperinsulinism/seizures
Tautan disimpan ke clipboard
Halaman 1 dari 153 hasil
Hyperinsulinism-hyperammonemia Syndrome in an Infant with Seizures.
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
Hyperinsulinism-hyperammonemia syndrome (HI/HA) is the second most common form of persistent hyperinsulinemic hypoglycemia of infancy (PHHI). The main clinical characteristics of HI/HA syndrome are repeated episodes of symptomatic hypoglycemia, but not usually severe. Consequently, children with
Seizures and diagnostic difficulties in hyperinsulinism-hyperammonemia syndrome.
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
Hyperinsulinism/hyperammonemia (HI/HA) syndrome is a rare disorder presented with recurrent hypoglycemia and elevated serum ammonia, which may lead to development delays, permanent neurologic damages, if it remains underdiagnosed. It is caused by activating mutations in the GLUD1 gene which encodes
Intractable absence seizures in hyperinsulinism-hyperammonemia syndrome.
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
A girl with intractable absence seizures and facial myoclonia at age 7 years was eventually diagnosed with hyperinsulinism-hyperammonemia syndrome because of hypoglycemia, hyperinsulinism, hyperammonemia, and the results of an oral l-leucine loading test. Her seizures occurred even during periods of
Seizure due to somatostatin analog discontinuation in a case diagnosed as congenital hyperinsulinism novel mutation.
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
The most common reason for refractory hypoglycemia in newborns is congenital hyperinsulinism. We report a girl with congenital hyperinsulinism due to novel homozygous mutation (c.2041-25 G>A; aberrant splicing mutation) in the ABCC8 gene encoding SUR1 and during somatostatin analog (octreotide)
Familial hyperinsulinism-hyperammonemia syndrome in a family with seizures: case report.
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
Hyperinsulinism-hyperammonemia (HI/HA) syndrome is the second most frequent cause of congenital hyperinsulinism (CHI) and it is characterized by recurrent symptomatic hypoglycemia and persistent hyperammonemia. We describe the familial case of a 2-year-old child and her 32-year-old mother who,
[Epileptiform seizures caused by hyperinsulinism in a 12 year old boy].
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
[Cerebral seizures in hyperinsulinism].
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
VERTIGINOUS TEMPORAL LOBE SEIZURES STIMULATED BY FUNCTIONAL HYPERINSULINISM.
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
The hitchhiker's guide to the role of (transient) hypoglycemia in refractory seizures and epilepsy.
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
Hypoglycemia and hypoglycorrhachia, although they are uncommon causes of refractory seizures and epilepsy, should always be considered because they are potentially treatable conditions. A high index of suspicion and low threshold for testing recurrent blood and at least one cerebrospinal fluid
[Persistent neonatal hyperinsulinism. Analysis of the differential diagnosis. Report of two cases].
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
Persistent neonatal hyperinsulinism is the most common cause of refractory hypoglycemia during the first year of life. Inadequate insulin secretion is associated to mutations of four different genes, that can be diagnosed to orient patient management. We report two patients: a female newborn that
Long-term neurodevelopmental outcome in conservatively treated congenital hyperinsulinism.
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
BACKGROUND
Congenital hyperinsulinism (CH) is treated surgically in many centers (near-total and partial pancreatectomy for diffuse and focal disease respectively). Most patients treated with near-total pancreatectomy developed diabetes during childhood/puberty. CH patients are at increased risk of
Clinical presentation and treatment response to diazoxide in two siblings with congenital hyperinsulinism as a result of a novel compound heterozygous ABCC8 missense mutation.
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
BACKGROUND
Congenital hyperinsulinism (CHI) can present with considerable clinical heterogeneity which may be due to differences in the underlying genetic etiology. We present two siblings with hyperinsulinaemic hypoglycaemia (HH) and marked clinical heterogeneity caused by compound heterozygosity
Persistent hyperinsulinemic hypoglycaemia followed as benign infantile convulsion.
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
An 18-month-old boy developed seizures at 3 months of age. He developed normally and, his EEG and brain CT revealed no abnormal findings. The blood sugar level was normal at that time, thus he was diagnosed as having benign infantile convulsion. At 7 months of age seizures reappeared, and
[Neonatal hypoglycemia caused by hyperinsulinism and subsequent epilepsy].
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
A historical cohort study was undertaken to determine the risk of epilepsy in a population of 18 newborns with neonatal hypoglycemia due to insulin excess. Follow-up was 3 years 8 months (range 7 years-1 year 3 months). Insulin excess was associated with maternal diabetes in 13 infants, with an
[Pitfalls in the diagnosis of congenital hyperinsulinism: a case report and review of the literature].
Hanya pengguna terdaftar yang dapat menerjemahkan artikel
Masuk daftar
BACKGROUND
Congenital hyperinsulinism is the most common cause for recurrent hypoglycaemia in neonates and infants. Uncontrolled hypoglycaemia leads to seizures and long-term cerebral damage. Often, the diagnosis is delayed because of nonspecific symptoms and confusing laboratory results.
METHODS
We
Database tanaman obat terlengkap yang didukung oleh sains
- Bekerja dalam 55 bahasa
- Pengobatan herbal didukung oleh sains
- Pengenalan herbal melalui gambar
- Peta GPS interaktif - beri tag herba di lokasi (segera hadir)
- Baca publikasi ilmiah yang terkait dengan pencarian Anda
- Cari tanaman obat berdasarkan efeknya
- Atur minat Anda dan ikuti perkembangan berita, uji klinis, dan paten
Ketikkan gejala atau penyakit dan baca tentang jamu yang mungkin membantu, ketik jamu dan lihat penyakit dan gejala yang digunakan untuk melawannya.
* Semua informasi didasarkan pada penelitian ilmiah yang dipublikasikan
