Results 1 to 10 of about 1,180,087 (300)

Congenital Abnormalities and Multiple Sclerosis [PDF]

BMC Neurology, 2010
Background There is a strong maternal parent-of-origin effect in determining susceptibility to multiple sclerosis (MS). One hypothesis is that an abnormal intrauterine milieu leading to impaired fetal development could plausibly also result in increased ...
Orton Sarah-Michelle, Dyment David A, Criscuoli Maria, Guimond Colleen, Ramagopalan Sreeram V, Yee Irene M, Ebers George C, Sadovnick Dessa   +7 more
doaj   +4 more sources

Chromosome 1q21 abnormalities in multiple myeloma [PDF]

Blood Cancer Journal, 2021
Gain of chromosome 1q (+1q) is one of the most common recurrent cytogenetic abnormalities in multiple myeloma (MM), occurring in approximately 40% of newly diagnosed cases.
Timothy M. Schmidt, Rafael Fonseca, Saad Z. Usmani   +2 more
doaj   +3 more sources

Multiple Congenital Heart Abnormalities [PDF]

Acta Medica Bulgarica, 2019
Congenital heart abnormalities are rare and most often occur separately. These structural and functional disorders can cause a range of diseases that vary in severity, from mild or even asymptomatic to severe and life-threatening.
Lazarov S., Bogdanov G., Nikolov R.
doaj   +2 more sources

Systemic multiple myeloma and colonic abnormalities

VideoGIE, 2023
Video 1Colonic abnormalities observed in the course of systemic multiple myeloma.
Katarzyna M. Pawlak, MD, PhD, MRCPUK, Kareem Khalaf, MD, Klaus Mönkemüller, MD, PhD, FJGES, Krzysztof Kurek, MD, PhD   +3 more
doaj   +3 more sources

Comparison of Intraspinal Abnormalities Prevalence in Congenital Scoliosis [PDF]

JBJS Open Access
Background:. The increasing utilization of magnetic resonance imaging has facilitated the detection of intraspinal abnormalities in congenital scoliosis (CS) caused by hemivertebra.
Li Jie, MD, PhD, Chen Chunxiao, MS, Qin Xiaodong, MD, PhD, Hu Zongshan, MD, PhD, Qiao Jun, MD, PhD, Mao Saihu, MD, PhD, Shi Benlong, MD, PhD, Qiu Yong, MD, PhD, Zhu Zezhang, MD, PhD, Liu Zhen, MD, PhD   +9 more
doaj   +2 more sources

NF1 with Multiple Cardiac Structural Abnormalities Leading to Cerebral Infarction [PDF]

Diagnostics
Background/Objectives: Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder driven by mutations in the NF1 gene, whose pathogenesis centers on the loss of neurofibromin function and subsequent hyperactivation of the RAS/MAPK pathway. Notably,
Jingwei Ye, Yiyi Jiang, Hanmin Wang, Dan Wang   +3 more
doaj   +2 more sources

Arthrogryposis: A Rare Manifestation in Infant of Diabetic Mother [PDF]

Online Journal of Health & Allied Sciences, 2009
Arthrogryposis multiplex congenita is characterized by non-progressive, multiple joint contractures present at birth. The major cause of arthrogryposis is fetal akinesia due to fetal abnormalities like neurogenic, muscle, connective tissue abnormalities ...
Amar M. Taksande, KY Vilhekar, Arvind Kumar   +2 more
doaj   +1 more source

Characterization of cytogenetic abnormalities in Lebanese multiple myeloma patients [PDF]

BMC Cancer
Background Multiple Myeloma (MM) is a hematological malignancy originating from the bone marrow and affecting the germinal lymphoid B cells, resulting in abnormal plasma cells and end organ damage.
Guitta Najem, Chloe Kharsa, Hampig Raphael Kourie, Joseph Kattan, Fadi Nasr, Fadi El Karak, Jad Wakim, Marwan Ghosn, Georges Chahine, Colette Hanna, Rachel El Ferkh, Chantal Farra, Alain Chebly   +12 more
doaj   +2 more sources

Anatomical mapping of vascular anomalies of the lips [PDF]

Revista Brasileira de Cirurgia Plástica, 2020
Introduction: The lip is the body region more often affected by vascular anomalies (VAs). Identifying the appropriate etiology of the lesion is significantly important when determining the treatment of choice for the patient.
Rafael Ferreira Zatz, Dov Charles Goldenberg, Vânia Kharmandayan, Esther Mihwa Choi, Rolf Gemperli   +4 more
doaj   +1 more source

Anatomic and histological characteristics of vagina reconstructed by McIndoe method [PDF]

Vojnosanitetski Pregled, 2009
Background/Aim. Congenital absence of vagina is known from ancient times of Greek. According to the literature data, incidence is 1/4 000 to 1/20 000. Treatment of this anomaly includes non-operative and operative procedures. McIndoe procedure uses split
Kozarski Jefta, Vesanović Svetlana, Bogdanović Zoran   +2 more
doaj   +1 more source