120: Rare Association of IgA Nephropathy and Lymphedema Distichiasis Syndrome: First Case Report

2009 ◽  
Vol 53 (4) ◽  
pp. B52
Keyword(s):  
Case Report ◽  
Iga Nephropathy ◽  
Rare Association ◽  
First Case

scholarly journals Cerebral Palsy with Nephrotic Syndrome : A Rare Association- First Case Report in Bangladesh

2015 ◽  
Vol 6 (2) ◽  
pp. 78-79
Author(s):  
Md Kabir Alam ◽  
Laila Yeasmin ◽  
Saukat Ara Begum ◽  
Anwar Hossain Khan ◽  
Mahbub Ul Alam ◽  
...  
Keyword(s):  
Nephrotic Syndrome ◽  
Cerebral Palsy ◽  
Case Report ◽  
International Medical ◽  
Medical College ◽  
Rare Association ◽  
First Case

Abstract not availableNorthern International Medical College Journal Vol.6(2) 2015: 78-79

scholarly journals A rare association of hepatitis A virus infection with type-1 diabetes

2016 ◽  
Vol 6 (2) ◽  
Author(s):  
Mohammed Hasosah ◽  
Alaa Bokhari ◽  
Ashraf Alsahafi ◽  
Ghassan Sukkar ◽  
Abdullah Alzaben
Keyword(s):  
Type 1 Diabetes ◽  
Case Report ◽  
Virus Infection ◽  
Liver Diseases ◽  
Hepatitis A ◽  
Hepatitis A Virus ◽  
Review Of The Literature ◽  
Rare Association ◽  
First Case

Patients with type-1 diabetes are predisposed to develop a spectrum of liver diseases, which includes fatty liver, steatohepatitis and cirrhosis. The association of hepatitis A infection with type-1 diabetes is extremely rare. To the best of our knowledge, our case is the first case report in children. We described a nine year-old girl who had type-1 diabetes and developed hepatitis A virus infection without complications. A review of the literature is also provided.

scholarly journals Myeloid bodies caused by COQ2 mutation: a case with the coincidence of COQ2 nephropathy and IgA nephropathy

2021 ◽  
Author(s):  
Hai-Feng Ni ◽  
Yan Yang ◽  
Chun-Qing Li ◽  
Tong-Zhou Zhou ◽  
Bi-Cheng Liu ◽  
...  
Keyword(s):  
Case Report ◽  
Fabry Disease ◽  
Iga Nephropathy ◽  
Curative Effect ◽  
Myeloid Bodies ◽  
Cationic Amphiphilic Drugs ◽  
First Case ◽  
Amphiphilic Drugs ◽  
Gla Gene ◽  
Coq10 Supplementation

Abstract IgA nephropathy (IgAN) combined with myeloid bodies have been reported in Fabry disease (FD). However, we excluded the diagnosis of FD by no mutation in GLA gene. And she denied the use of cationic amphiphilic drugs. Interestingly, we identified a novel missense mutation for COQ2, which can cause COQ2 mutation associated nephropathy. The patient we reported also had heteromorphic mitochondria, and a good curative effect after CoQ10 supplementation. Combined these, this patient was diagnosed with COQ2 nephropathy and IgAN. To our knowledge, this is the first case report that COQ2 nephropathy with pathologic manifestations of myeloid body in podocytes.

The first case report of Pembrolizumab inducing thyroiditis and hypophysitis

2020 ◽  
Author(s):  
Rahman Maraqa Sima Abdel ◽  
Robert McMahon ◽  
Anusha Pinjala ◽  
Gastelum Alheli Arce ◽  
Mohsen Zena
Keyword(s):  
Case Report ◽  
First Case

Harel-Yoon syndrome: the first case report from Saudi Arabia

2020 ◽  
pp. 22-27 ◽  
Author(s):  
Alaa AlAyed ◽  
Manar Samman ◽  
Abdul Peer-Zada ◽  
Mohammed Almannai
Keyword(s):  
Saudi Arabia ◽  
Case Report ◽  
First Case

Case Report: Management of a Patient with mTBI and Vestibular Hypofunction with the Binasal Occlusion Technique

2018 ◽  
pp. 87-90
Keyword(s):  
Case Report ◽  
Visual Motion ◽  
Hand Movement ◽  
Motion Sensitivity ◽  
Vestibular Hypofunction ◽  
First Case ◽  
Neurological Exam ◽  
History Of ◽  
Occlusion Technique ◽  
Visual Vertigo

Background: Binasal Occlusion (BNO) is a clinical technique used by many neurorehabilitative optometrists in patients with mild traumatic brain injury (mTBI) and increased visual motion sensitivity (VMS) or visual vertigo. BNO is a technique in which partial occluders are added to the spectacle lenses to suppress the abnormal peripheral visual motion information. This technique helps in reducing VMS symptoms (i.e., nausea, dizziness, balance difficulty, visual confusion). Case Report: A 44-year-old AA female presented for a routine eye exam with a history of mTBI approximately 33 years ago. She was suffering from severe dizziness for the last two years that was adversely impacting her ADLs. The dizziness occurred in all body positions and all environments throughout the day. She was diagnosed with vestibular hypofunction and had undergone vestibular therapy but reported little improvement. Neurological exam revealed dizziness with both OKN drum and hand movement, especially in the left visual field. BNO technique resulted in immediate relief of her dizziness symptoms. Conclusion: To our knowledge, this is the first case that illustrates how the BNO technique in isolation can be beneficial for patients with mTBI and vestibular hypofunction. It demonstrates the success that BNO has in filtering abnormal peripheral visual motion in these patients.

Anesthesia in Carvajal syndrome; the first case report

2020 ◽  
Vol 24 (1) ◽  
pp. 105-107
Author(s):  
Sedighe Shahhosseini ◽  
Reza Aminnejad ◽  
Amir Shafa ◽  
Mehrdad Memarzade
Keyword(s):  
Intensive Care ◽  
Case Report ◽  
Surgical Resection ◽  
Genetic Disorder ◽  
Anesthetic Technique ◽  
Close Monitoring ◽  
Anesthesia Management ◽  
Rare Genetic Disorder ◽  
First Case ◽  
Anesthetic Considerations

Carvajal syndrome is a rare genetic disorder. Patients reporting for surgery pose some difficulties in anesthesia management. In this case report we present the case of a 12-year-old boy, who was a known case of Carvajal syndrome, referred for surgical resection of perianal condyloma. Close monitoring of hemodynamic status is the mainstay of anesthetic considerations in such patients. As in any other challenging scenario, it should be kept in mind that ‘there is no safest anesthetic agent, nor the safest anesthetic technique; there is only the safest anesthesiologist’. Citation: Shahhosseini S, Aminnejad R, Shafa A, Memarzadeh M. Anesthesia in Carvajal syndrome; the first case report. Anaesth pain intensive care 2020;24(1):___ DOI: https://doi.org/10.35975/apic.v24i1.

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