Clinical case 3: The H Syndrome
Diagnostic value of whole-body MRI in Opsoclonus-myoclonus syndrome: a clinical case series (3 case reports)
... Discussion and conclusions OMS is a rare pediatric disease, which poses significant challenge to the caregiving physicians. We report on three patients who presented with OMS due to an underlying neuroblastic tumor. In ...
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Brocq lyell syndrome induced by phenytoin Clinical case
... a clinical case of NET in a 27-year-old woman, with the use of anticonvulsant drugs (phenytoin) as a possible etiological factor involved in this ...the case we present, phenytoin therapy for 11 days ...
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Clinical features and imaging findings in a case of Capgras syndrome
... “illusion des sosies”. 7 The Capgras delusion can be consid- ered a symptom occurring in adults and in children 8 in the context of both psychiatric and organic illness. 9,10 As a matter of fact, it can be associated ...
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Cobb Syndrome: A Case Report with Review of Clinical and Imaging Findings
... Our case serves to point out several encountered pitfalls before arriving at the correct ...this case was the combination of a vascular skin lesion in a dermatomal distribution on physical exam and atypical ...
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Prosthodontic management of a patient with combination syndrome: a clinical case report
... a syndrome are interlinked to one another progressing in a sequential manner is known as combination syndrome by Ellsworth Kelly in ...This syndrome poses a considerable challenge to ...the ...
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The Rehabilitation of a Susac Syndrome Patient: A Case Report and Clinical Review
... side with significant cochlear [31]. Hence, vestibular rehabilitation of the patient is a crucial aspect of the rehabilitation plan. Vestibular rehabilitation is based on improving the natural phenomenon called ...
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Clinical Approach to a Suspected Case of First Branchial Arch Syndrome
... arch syndrome is a congenital disorder characterized by a wide spectrum of anomalies in the first branchial arch, mainly affecting the lower jaw, ear, or mouth, during early embryonic ...suspected case of ...
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Hepatomegaly and type 1 diabetes: a clinical case of Mauriac’s syndrome
... s syndrome is a rare disease, which includes short stature, growth maturation delay, dyslipidemia, moon facies, protuberant abdomen, hepatomegaly with transaminase ...s syndrome in both adults and children ...
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A Case Report of Mucopolysaccharidosis Type 1 (MPS I H - Hurler Syndrome)
... specific clinical and radiological features, mucopolysaccharidosis type 1 was suspected, and for confirmation of diagnosis, enzyme assay was sent, which showed low levels of α-L- iduronidase, ...
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Clinical Case Report HYPERSEXUALITY AND DYSEXECUTIVE SYNDROME AFTER A THALAMIC INFARCT
... This case presents strong evidence of a thalamic infarct. The acute onset and immediate sequelae are indicative of a stroke, combined with the cerebral angiogram and presence of ventricular blood. The continued ...
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Challenges in clinical and laboratory diagnosis of androgen insensitivity syndrome: a case report
... feminization syndrome) have female external genitalia, blind vaginas, an absent uterus and female adnexa, female breast development, and abdominal or inguinal ...
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Antiphospholipid syndrome: a case report with an unusual wide spectrum of clinical manifestations
... A 43 years old man was admitted to our Internal Medi- cine Unit on April 2018 with a 7 days history of low- grade fever, bilateral epistaxis and abdominal pain. His personal medical history showed that 9 years ear- lier ...
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Rosselli-Gulienetti Syndrome: Clinical Presentation and Management – A Rare Case Report
... On clinical examination, both maxillary and mandibular edentulous arches were found to be severely resorbed with loss of alveolar bone in the maxillary anterior region [Figure ...
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Case Report Mowat-Wilson syndrome: clinical and molecular report of the first case in mainland China
... Mowat-Wilson syndrome (MWS, MIM #235730) is a rare genetic disorder characterized by moderate-to- severe mental retardation, a recognizable facial gestalt and multiple congenital ...
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Sandifer’s Syndrome in a 3 Month Old Male Infant: A Case Report
... Barium swallow/meal examination revealed GER without evidence of hiatus hernia (Figure 2). Twenty-four hours of pH monitoring was not done, due to the lack of availability in our hospital. Therefore, the diagnosis, in ...
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Case Report: Clinical and Diagnostic Aspects of Mayer Rokitansky Kuster Hauser Syndrome
... Mayer-Rokitansky-Kuster-Hauser Syndrome (MRKH) is a rare disease cha- racterized by total or partial vagina agenesis, karyotype 46, XX with normal secondary sexual ...the syndrome to be diagnosed only after ...
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Pharmacokinetics-based clinical management of acquired von Willebrand syndrome: a case report
... Willebrand syndrome levels tested 1 hour after completion of IVIG had improved to 82%, confirming the diagnosis of MGUS-induced AVWS and indicating that adsorption of VWF on thyroid cancer cells was not a major ...
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Kartagener syndrome. Late clinical diagnosis and some of its consequences. Presentation of a case
... bronchiectasis, recurrent respiratory infections, a history of infertility and evidence of dextrocardia, bronchiectasis and sinusitis, thus establishing the diagnosis of this syndrome of low prevalence in the ...
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Alagille syndrome: clinical perspectives
... 20p12.2 microdeletion The presence of developmental delay and/or hearing loss in addition to the features commonly seen in ALGS may increase the suspicion of chromosome 20p12.2 interstitial microdeletion, which ...
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Burnout is a clinical syndrome characterized
... found that 86.9 percent of respondents reported physical discomfort or symptoms attributable to performing laparoscopy. Not surprisingly, surgeon age and laparoscopic case volume positively correlated with ...
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