نتایج جستجو برای: poikiloderma with neutropenia syndrome
تعداد نتایج: 9376087 فیلتر نتایج به سال:
From the Pulmonary and Critical Care Medicine Division, Department of internal Medicine, the Department of Pathology, and the Department of Epidemiology, School of Public Health, University of Michigan Medical Center, Ann Arbor, Michigan. This work was supported in part by the National Heart, Lung, and Blood Institute (HL31963) and by the American Heart Association with funds contributed in par...
PURPOSE In this study, we aimed to investigate the perinatal clinical conditions of very low birth weight (VLBW) infants born to mothers with pregnancy-induced hypertension (PIH) focusing on the effects of early postnatal neutropenia. METHODS We reviewed the medical records of 191 VLBW infants who were born at Konyang University Hospital, between March 2003 and May 2011. We retrospectively an...
Cutaneous hyperpigmentations are frequent complaints, motivating around 8.5% of all dermatological consultations in our country. They can be congenital, with different patterns of inheritance, or acquired in consequence of skin problems, systemic diseases or secondary to environmental factors. The vast majority of them are linked to alterations on the pigment melanin, induced by different mecha...
The mechanism of neutropenia in Felty's Syndrome (FS) was tested. The suppressor capacity of mononuclear cells from patients with FS on normal bone marrow granulopoiesis was tested by the in vitro colony forming unit in culture assay. Peripheral blood, bone marrow, and spleen cells from FS patients with marked neutropenia (less than 1,000 neutrophils/mm3) suppressed the colony forming unit in c...
Bacterial infection following major burn injury leads to neutrophile dysfunction and neutropenia which results in serious sepsis. Administration of graolocyte-colon specific factor (G-CSF) is useful for treatment of neutropenia and decreasing the complications of severe infection following burn injuries. A 2- year old boy with major burn injury, despite administration of broad spectrum antibi...
OBJECTIVE To investigate the clinical, genetic, and laboratory features of 26 patients with Kindler syndrome. DESIGN Case series of patients recruited when they were seen at outpatient consultations in the Department of Dermatology at the Changuinola Hospital in Bocas del Toro, Panama, between May 1986 and December 1990. SETTING Clinical history, physical examination, and laboratory studies...
Neonatal lupus syndrome is a rare disease. The manifestations of this disease in neonatal period include congenital heart block, cutaneous leasions, liver disease, thrombocytopenia, Neutropenia, pulmonary and nurologic derangements. Most of the clinical manifestations ofter disappear spontaneously. Although congenital heart block is usually permanent, and often require pacemakers. Congenital he...
Breast Cancer (BC) has associated risk factors and genetic factors like BRCA1, and BRCA2. Many benign and malignant disease processes are found concurrently with BC and believed to be additional risk factors like gall bladder stones (cholelithiasis), hypertension, diabetes mellitus, cerebrovascular lesions, arthritis, spine and spinal cord degenerative lesions, infertility, depression, sleep di...
GATA2 deficiency-formerly described as MonoMAC syndrome; dendritic cells, monocytes, B cells, and natural killer cell deficiency; familial myelodysplastic syndrome/acute myeloid leukemia; or Emberger syndrome-encompasses a range of hematologic and nonhematologic anomalies, mainly characterized by monocytopenia, B lymphopenia, natural killer cell cytopenia, neutropenia, immunodeficiency, and a h...
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