scholarly journals Autosomal Recessive Cutis Laxa Type 1: A Rare Case Report

2019 ◽  
Vol 7 (8) ◽  
Author(s):  
Saru Thakur ◽  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Autosomal Recessive ◽  
Cutis Laxa ◽  
Rare Case Report

Acquired cutis laxa secondary to Sweet syndrome in a child (Marshall syndrome): A rare case report

2019 ◽  
Vol 47 (2) ◽  
pp. 146-149
Author(s):  
Ashish Jagati ◽  
Shivank Shrivastava ◽  
Bhavna Baghela ◽  
Pooja Agarwal ◽  
Siddhartha Saikia
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Cutis Laxa ◽  
Sweet Syndrome ◽  
Rare Case Report

scholarly journals A rare case report of neurofibromatosis type 1 in a 12-year-old child: A 15-month follow-up

2020 ◽  
Vol 24 (4) ◽  
pp. 106
Author(s):  
Srinivas Nallanchakrava ◽  
ManojKumar Mallela ◽  
VShiva Kumar Jeenepalli ◽  
HM Niharika
Keyword(s):  
Case Report ◽  
Neurofibromatosis Type 1 ◽  
Rare Case ◽  
Neurofibromatosis Type ◽  
Rare Case Report

scholarly journals An observation of autosomal recessive hyper-IgE syndrome: a rare case report

2017 ◽  
Vol 104 (6) ◽  
pp. 676-679
Author(s):  
Tasleem Arif ◽  
Mohammad Adil ◽  
Syed Suhail Amin ◽  
Konchok Dorjay
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Autosomal Recessive ◽  
Hyper Ige Syndrome ◽  
Rare Case Report

Excessive Blood Glucose in Diabetic Ketoacidosis and Hyperosmolar Hyperglycemia: A Rare Case Report

2021 ◽  
Author(s):  
Alireza Kashanizadeh ◽  
Ahmad Reza Salmanpour ◽  
Nasim Shirin Sahrae ◽  
Mohammad Firoozbakht ◽  
Hamid Karimi
Keyword(s):  
Risk Factors ◽  
Case Report ◽  
Diabetic Ketoacidosis ◽  
Rare Case ◽  
Insulin Production ◽  
Β Cells ◽  
Pancreatic Β Cells ◽  
Rare Case Report ◽  
Hyperosmolar Hyperglycemic State

Type 1 diabetes (T1D) is an autoimmune assault on pancreatic β-cells characterized by a decrease in insulin production. The worldwide incidence rate of T1D is reportedly increasing. In parallel with the increase of T1D, diabetic ketoacidosis (DKA) and hyperosmolar hyperglycemic state (HHS) also appear as two risk factors for hyperglycemia. This case report presents a T1D patient with DKA and HHS who was finally discharged after recovery.

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