Български
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)
osteopetrosis/епилептични припадъци
Линкът е запазен в клипборда
Страница 1 от 17 резултата
Hypocalcemia presenting with multifocal seizure in a baby with osteopetrosis.
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Hypocalcemia presenting with multifocal seizure in a baby with osteopetrosis.
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Severe neuronopathic autosomal recessive osteopetrosis due to homozygous deletions affecting OSTM1.
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Autosomal recessive osteopetrosis (ARO, MIM 259700) is a genetically heterogeneous rare skeletal disorder characterized by failure of osteoclast resorption leading to pathologically increased bone density, bone marrow failure, and fractures. In the neuronopathic form neurological complications are
Osteopetrosis; a report of two Iranian patients with autosomal recessive inheritance pattern.
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
In the rare hereditary bone disorder of osteopetrosis, reduced bone resorption function leads to both the development of densely sclerotic fragile bones and progressive obliteration of the marrow spaces and cranial foramina. Marrow obliteration, typically associated with extramedullary hemopoiesis
Infantile Malignant Osteopetrosis: Delay in Diagnosis Eliminates Chance of Cure.
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
A 4.5 year-old girl presented with abdominal distention, failure to thrive, visual and hearing loss. In her medical history there was meningitis in the neonatal period, convulsions, enlargement of her head, nistagmus and exophtalmus at the tenth month. When she was 15 month-old, she had
A Rare Case of Malignant Infantile Osteopetrosis Presenting as Frontal Lobe Hemorrhage
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Osteopetrosis comprises a group of rare inherited disorders of the bones characterized by a common radiographic finding of increased bone thickness. The disorders vary genetically as well as clinically, and range in severity from mild manifestations to fatal complications based on the type of the
Brain Abscess in a Patient with Osteopetrosis: A Rare Complication
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Brain abscess formation is extremely rare in patients with osteopetrosis. Herein, we report a case of viridans streptococci brain abscess in an immunocompromised child diagnosed with osteopetrosis. The patient presented with a sudden change in mental status and convulsions. Radiological evaluation
Osteopetrosis. Current clinical considerations.
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Osteopetrosis is an inherited skeletal condition characterized by increased bone radiodensity. There are three clinical groups: infantile-malignant autosomal recessive, fatal within the first few years of life (in the absence of effective therapy); intermediate autosomal recessive, appears during
Clinical and cellular manifestations of OSTM1-related infantile osteopetrosis.
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Infantile ARO is a genetic disorder characterized by osteoclast dysfunction that leads to osteopetrosis. We describe a novel mutation affecting the OSTM1 locus responsible for ARO. In addition to common clinical features of osteopetrosis, the patient developed a unique neuronal pathology that
The association of infantile osteopetrosis and neuronal storage disease in two brothers.
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Neurological manifestations in infantile osteopetrosis are common and varied, and not always attributable to the skeletal pathology. An unusual association of osteopetrosis with neuronal storage of ceroid lipofuscin is reported in two infant brothers born of nonconsanguinous parents. The first child
[Juvenile malignant osteopetrosis. Clinico-radiological study of 7 cases].
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Clinical and radiological studies of seven patients with autosomic recessive malignant osteopetrosis are presented. Diagnosis was established before the age of 3 months in six cases and at 7 months in one. In all cases the presenting signs were pallor and hepatosplenomegaly with associated
Osteopetrosis.
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Osteopetrosis ("marble bone disease") is a descriptive term that refers to a group of rare, heritable disorders of the skeleton characterized by increased bone density on radiographs. The overall incidence of these conditions is difficult to estimate but autosomal recessive osteopetrosis (ARO) has
Infantile malignant osteopetrosis: a rare cause of neonatal hypocalcemia.
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Infantile malignant osteopetrosis (IMO; OMIM 259700) is a rare inherited bone disease characterized by reduced or dysregulated activity of osteoclasts, resulting in generalized osteosclerosis. The disease usually presents within the first few months of life with anemia, hepatosplenomegaly, frontal
Malignant infantile osteopetrosis presenting with neonatal hypocalcaemia.
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Presentation characteristics were reviewed in 14 children from 12 families with malignant infantile osteopetrosis seen at two large referral centres for bone marrow transplantation. Children from six of these families presented initially with symptoms of hypocalcaemia. These comprised early or late
A case report of dysosteosclerosis observed from the prenatal period.
Само регистрирани потребители могат да превеждат статии
Вход / Регистрация
Dysosteosclerosis is a sclerosing bone dysplasia with skeletal changes resembling those of osteopetrosis. The disorder is associated with dental anomalies and occasionally mental retardation. Because of the rarity and phenotypic diversity of dysosteosclerosis, it remains unsolved whether or not the
Най-пълната база данни за лечебни билки, подкрепена от науката
- Работи на 55 езика
- Билкови лекове, подкрепени от науката
- Разпознаване на билки по изображение
- Интерактивна GPS карта - маркирайте билките на място (очаквайте скоро)
- Прочетете научни публикации, свързани с вашето търсене
- Търсете лечебни билки по техните ефекти
- Организирайте вашите интереси и бъдете в крак с научните статии, клиничните изследвания и патентите
Въведете симптом или болест и прочетете за билките, които биха могли да помогнат, напишете билка и вижте болестите и симптомите, срещу които се използва.
* Цялата информация се базира на публикувани научни изследвания
