CONGENITAL METHEMOGLOBINEMIA TYPE 2 - A RARE CASE REPORT

2017 ◽  
Vol 14 (2) ◽  
Author(s):  
Shinas Nellicka ◽  
Abraham John ◽  
Vivin Abraham
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Case Report

scholarly journals Acquired generalized lipodystrophy type 2-lawrence syndrome: a rare case report

2020 ◽  
Vol 7 (2) ◽  
pp. 437
Author(s):  
Dhanalakshmi K. ◽  
Mohinish S. ◽  
Dakshayani B. ◽  
Mallesh K.
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Acanthosis Nigricans ◽  
Rare Disorder ◽  
Rare Occurrence ◽  
Rare Case Report ◽  
Systemic Manifestations

Lawrence syndrome (Acquired Generalized Lipodystrophy) is a rare disorder, characterized by various dermatological and systemic manifestations such as lipodystrophy, hypertriglyceridemia, hepatomegaly, acanthosis nigricans and acromegaloid features. Because of its rare occurrence we are reporting a case with similar manifestations in a 10 years old child.

scholarly journals Melioidosis complicating lepromatous leprosy with type 2 lepra reaction: A rare case report from India

2019 ◽  
Vol 90 (4) ◽  
pp. 450-455
Author(s):  
Swetalina Pradhan ◽  
Arpita Nibedita Rout ◽  
Chandra Sekhar Sirka ◽  
Sanjib Kumar Das ◽  
Kananbala Sahu
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Lepromatous Leprosy ◽  
Rare Case Report

scholarly journals Caliber persistent artery in the anterior palate of an Egyptian patient with type-2 diabetes mellitus: a rare case report

2017 ◽  
Vol 11 (1) ◽  
pp. 61
Author(s):  
Bacem A.E.O. Khalele
Keyword(s):  
Diabetes Mellitus ◽  
Type 2 Diabetes ◽  
Type 2 Diabetes Mellitus ◽  
Case Report ◽  
Rare Case ◽  
Ulcerative Lesion ◽  
Diagnostic Dilemma ◽  
Rare Case Report ◽  
Egyptian Patient

This paper reports a very rare case of isolated ulcerative lesion of the palate in a patient with type-2 diabetes mellitus. The patient refused to run any radiological tests, other than the periapical radiograph. This rendered the diagnostic dilemma more challenging. Through histochemical and immunohistochemical stains, the case could be non-invasively diagnosed as caliberpersistent artery. All differential diagnoses were excluded based on concrete findings.

Primary neuroendocrine carcinoma of renal: a rare case report

2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko
Keyword(s):  
Case Report ◽  
Neuroendocrine Carcinoma ◽  
Rare Case ◽  
Rare Case Report

Combination of turner syndrome and congenital adrenal hyperplasia: a rare case report

2017 ◽  
Author(s):  
Ivana Sagova ◽  
Dušan Pavai ◽  
Matej Stančik ◽  
Helena Urbankova ◽  
Juliana Gregova ◽  
...  
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Turner Syndrome ◽  
Rare Case ◽  
Adrenal Hyperplasia ◽  
Rare Case Report
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