scholarly journals Corrigendum to “Chromosome 3p Inverted Duplication with Terminal Deletion: Second Postnatal Case Report with Additional Clinical Features”

2019 ◽  
Vol 2019 ◽  
pp. 1-1
Author(s):  
Jacquelyn D. Riley ◽  
Catherine M. Stefaniuk ◽  
Francine Erenberg ◽  
Angelika L. Erwin ◽  
Lauren Palange ◽  
...  
Keyword(s):  
Case Report ◽  
Clinical Features ◽  
Terminal Deletion ◽  
Chromosome 3P ◽  
Inverted Duplication

Ectodermal Dysplasia in two siblings: A Case report.

2019 ◽  
Author(s):  
CHAITHRA KALKUR ◽  
NILOFER HALIM ◽  
ANUSHA RANGARE ◽  
Rumisha .
Keyword(s):  
Case Report ◽  
Key Words ◽  
Clinical Features ◽  
Ectodermal Dysplasia ◽  
Heterogeneous Group ◽  
Eccrine Glands ◽  
Key Words Ectodermal Dysplasia

Ectodermal dysplasia is a heterogeneous group of inherited disorder affecting two or more ectodermally derived tissues such as skin, hair, nails, eccrine glands and teeth. The disorder is of two types: Hypohydrotic ectodermal dysplasia/Christ seimens –Touraine syndrome and Hydrotic ectodermal dysplasia/clousten syndrome. Commonly associated signs include hypohidrosis, anomalous dentition, onychodysplasia, hypotrichosis. Multidisciplinary approaches are required for optimal treatment3. Here, we present two cases of 19 and 13 year old male siblings who were diagnosed with the disorder based upon their clinical features. Key Words: ectodermal dysplasia, hypodontia; anomalous dentition.

scholarly journals Lupus Miliaris Disseminatus Faciei versus Granulomatous Rosacea: A Case Report

2021 ◽  
pp. 321-329
Author(s):  
Ji-In Seo ◽  
Min Kyung Shin
Keyword(s):  
Case Report ◽  
Case Studies ◽  
Clinical Features ◽  
Scar Formation ◽  
Accurate Diagnosis ◽  
Delayed Treatment ◽  
Inflammatory Dermatoses ◽  
Granulomatous Rosacea

Lupus miliaris disseminatus faciei (LMDF) and granulomatous rosacea are 2 distinct inflammatory dermatoses with overlapping clinical features: reddish-yellow papular eruptions localized on the central face. Consequently, LMDF can easily be misdiagnosed as granulomatous rosacea or vice versa. Because delayed treatment in LMDF may increase chances of permanent scar formation, accurate diagnosis is important. We therefore analyzed published literature and case studies to organize the essential features differentiating LMDF from granulomatous rosacea. In addition, we report each case of LMDF and granulomatous rosacea for direct comparison.

Terminal deletion 6P23: A case report

1990 ◽  
Vol 37 (4) ◽  
pp. 475-477 ◽  
Author(s):  
M. H. Kormann-Bortolotto ◽  
L. M. S. Farah ◽  
D. Soares ◽  
M. Corbani ◽  
R. Müller ◽  
...  
Keyword(s):  
Case Report ◽  
Terminal Deletion

scholarly journals Systemic scleroderma and lupus panniculitis with atypical clinical features: A case report and comprehensive review

2018 ◽  
Vol 4 (8) ◽  
pp. 789-793 ◽  
Author(s):  
Aaron R. Mangold ◽  
Collin M. Costello ◽  
Helen J.L. Cumsky ◽  
David J. DiCaudo ◽  
W. Leroy Griffing ◽  
...  
Keyword(s):  
Case Report ◽  
Clinical Features ◽  
Systemic Scleroderma ◽  
Comprehensive Review ◽  
Lupus Panniculitis

scholarly journals Clinical features, histopathological analysis and surgical treatment of a free floating vitreous cyst: a case report

2006 ◽  
Vol 69 (5) ◽  
pp. 753-755 ◽  
Author(s):  
Rodrigo Pessoa Cavalcanti Lira ◽  
Patrícia Jungmann ◽  
Luis Felipe Lynch de Moraes ◽  
Ana Paula Teles Silveira
Keyword(s):  
Case Report ◽  
Surgical Treatment ◽  
Clinical Features ◽  
Histopathological Analysis ◽  
Vitreous Cyst

scholarly journals Artery of Percheron infarction: review of literature with a case report

2015 ◽  
Vol 49 (2) ◽  
pp. 141-146 ◽  
Author(s):  
Urska Lamot ◽  
Ivana Ribaric ◽  
Katarina Surlan Popovic
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Clinical Features ◽  
Cerebral Circulation ◽  
Brain Ct ◽  
Ischemic Infarction ◽  
Artery Of Percheron ◽  
Imaging Approach ◽  
Intracranial Arteries ◽  
Posterior Cerebral Circulation

Abstract Background. Clinical features indicating an ischemic infarction in the territory of posterior cerebral circulation require a comprehensive radiologic examination, which is best achieved by a multi-modality imaging approach (computed tomography [CT], CT-perfusion, computed tomography angiography [CTA], magnetic resonance imaging [MRI] and diffusion weighted imaging [DWI]). The diagnosis of an acute ischemic infarction, where the damage of brain tissue may still be reversible, enables selection of appropriate treatment and contributes to a more favourable outcome. For these reasons it is essential to recognize common neurovascular variants in the territory of the posterior cerebral circulation, one of which is the artery of Percheron. Case report. A 69 year-old woman, last seen awake 10 hours earlier, presented with two typical clinical features of the artery of Percheron infarction, which were vertical gaze palsy and coma. Brain CT and CTA of neck and intracranial arteries upon arrival were interpreted as normal. A new brain CT scan performed 24 hours later revealed hypodensity in the medial parts of thalami. Other imaging modalities were not performed, due to the presumption that the window for the application of effective therapy was over. The diagnosis of an artery of Percheron infarction was therefore made retrospectively with the re-examination of the CTA of neck and intracranial arteries. Conclusions. A multi-modality imaging approach is necessary in every patient with suspicion of the posterior circulation infarction immediately after the onset of symptoms, especially in cases where primary imaging modalities are unremarkable and clinical features are severe, where follow-up examinations are indicated.

scholarly journals Primary Osteosarcoma of the Breast: A Case Report

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Anna Rizzi ◽  
Alberto Soregaroli ◽  
Claudia Zambelli ◽  
Fausto Zorzi ◽  
Stefano Mutti ◽  
...  
Keyword(s):  
Case Report ◽  
Adjuvant Chemotherapy ◽  
Soft Tissue ◽  
Clinical Features ◽  
Optimal Treatment ◽  
Skeletal System ◽  
Case Presentation ◽  
Primary Osteosarcoma ◽  
Haematogenous Spread ◽  
Tissue Form

Introduction. Primary osteosarcoma of the breast is a rare soft-tissue form of osteosarcoma without involvement of the skeletal system. Due to the rarity of the disease, its clinical features and optimal treatment remain unclear.Case Presentation. This case report deals with a 62-year-old woman with pure osteosarcoma of the breast.Conclusions. The prognosis of primary osteosarcoma of the breast is poor. Recurrence is frequent, and it is often associated with haematogenous spread of the disease to the lung. Treatment follows the model of sarcomas affecting other locations and must be planned in a multidisciplinary fashion. Adjuvant chemotherapy should be considered for patients with tumors showing aggressive features.

scholarly journals Recurrent Rash Secondary to Shiitake Dermatitis

2021 ◽  
Vol 8 (3) ◽  
Author(s):  
Nguyen L ◽  
◽  
Prodanovic E ◽  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Clinical Features ◽  
Relevant Literature ◽  
Cutaneous Reaction ◽  
Shiitake Mushrooms ◽  
Cutaneous Reactions

Ingestion of shiitake mushrooms can result in a cutaneous reaction known as shiitake dermatitis. In this case report, a recurrent rash in a 56-yearold female patient was found to be shiitake dermatitis. The clinical features, histology, and relevant literature are discussed in the context of differentiating shiitake dermatitis from other similar cutaneous reactions.

scholarly journals A 13-year-old Female with Bardet- Biedl Syndrome - A Case Report

2015 ◽  
Vol 26 (1) ◽  
pp. 31-34
Author(s):  
Syed Nesar Ahmed ◽  
Md Abu Shahin ◽  
Romal Chowdhury ◽  
Alamgir Mustak Ahammad ◽  
Md Nahiduzzaman Shazzad ◽  
...  
Keyword(s):  
Case Report ◽  
Retinitis Pigmentosa ◽  
Rare Disease ◽  
Clinical Features ◽  
Night Blindness ◽  
Learning Difficulties ◽  
Laboratory Findings ◽  
Bardet Biedl Syndrome

Bardet Biedl syndrome is a rare disease. A case report is presented here where a 13 years old girl presented with obesity, night blindness, learning difficulties and polydactyly. Obesity and night blindness started from since childhood. Her milestones of development were normal but having some learning difficulties. Her parents are healthy as well as her siblings. On examination she looks apathy, extreme obese, having polydactyly and retinitis pigmentosa and high B.P. On laboratory findings there is only dyslipidaemia. On the basis of clinical features she was diagnosed as a case of Bardet-Biedl syndrome.Bangladesh J Medicine Jan 2015; 26 (1) : 31-34

Sign in / Sign up

Export Citation Format

Share Document