scholarly journals CRIGGLER - NAJAR SYNDROME TYPE II IN PREGNANCY: A RARE CASE REPORT

2015 ◽  
Vol 4 (68) ◽  
pp. 11921-11923
Author(s):  
Richa Suresh Sankhe ◽  
Ganesh A Shinde ◽  
Jeena Pavithran
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Syndrome Type ◽  
Type Ii ◽  
Rare Case Report ◽  
In Pregnancy

scholarly journals 516 A Very Rare Case Report of Hermansky-Pudlak Syndrome Type ii

2012 ◽  
Vol 97 (Suppl 2) ◽  
pp. A150-A150
Author(s):  
G. Karasu ◽  
M. Inalhan ◽  
F. Yildiz ◽  
O. Temel ◽  
O. Arslan ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Syndrome Type ◽  
Type Ii ◽  
Rare Case Report ◽  
Hermansky Pudlak Syndrome

scholarly journals A Rare Case Report of Crigler Najjar Syndrome Type II

Cureus ◽  
2021 ◽  
Author(s):  
Eusha Abdul Raffay ◽  
Ayesha Liaqat ◽  
Maria Khan ◽  
Ali I Awan ◽  
Bakhat Mand
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Syndrome Type ◽  
Type Ii ◽  
Rare Case Report

scholarly journals Osteopetrosis in pregnancy: a rare case report

2011 ◽  
Vol 5 (1) ◽  
pp. 27-29
Author(s):  
Michaela Peer ◽  
Keelin O'Donoghue
Keyword(s):  
Case Report ◽  
Bone Mass ◽  
Rare Case ◽  
Rare Condition ◽  
Type Ii ◽  
Genetic Syndrome ◽  
Skeletal Fragility ◽  
Rare Case Report ◽  
Pregnancy And Delivery ◽  
In Pregnancy

Osteopetrosis is a genetic syndrome characterized by the failure of osteoclasts to resorb bone. This leads to skeletal fragility despite increased bone mass, with fractures, dental abscesses, osteoarthritis and scoliosis being the most common complications. There are few reports of patients with type II osteopetrosis undergoing pregnancy and delivery. This case outlines the management of pregnancy and a successful delivery in a woman with this rare condition.

Oral features of Griscelli syndrome type II: A rare case report

2018 ◽  
Vol 38 (6) ◽  
pp. 421-425
Author(s):  
Nitesh Tewari ◽  
Anju Rajwar ◽  
Vijay Prakash Mathur ◽  
Prabhat Kumar Chaudhari
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Syndrome Type ◽  
Type Ii ◽  
Griscelli Syndrome ◽  
Rare Case Report

scholarly journals PULMONARY ALVEOLAR MICROLITHIASIS IN PREGNANCY: A RARE CASE REPORT

2015 ◽  
Vol 4 (98) ◽  
pp. 16387-16389
Author(s):  
Hemanta Kumar Sethy ◽  
Biswal Pradipta Trilochan ◽  
Geetanjali Panda ◽  
Milan Misra
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Pulmonary Alveolar Microlithiasis ◽  
Rare Case Report ◽  
Alveolar Microlithiasis ◽  
In Pregnancy

scholarly journals Hypergammaglobulinemic Purpura of Waldenstrom (HGPW) in Pregnancy: A Rare Case Report

2018 ◽  
Vol 69 (S1) ◽  
pp. 24-27
Author(s):  
Renuka Malik ◽  
Avani Goyal ◽  
Veena Ganju ◽  
Kabir Sardana
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Case Report ◽  
Hypergammaglobulinemic Purpura ◽  
In Pregnancy

scholarly journals Case report: a rare case of Hunter syndrome (type II mucopolysaccharidosis) in a girl

2019 ◽  
Vol 20 (1) ◽  
Author(s):  
A. N. Semyachkina ◽  
E. Y. Voskoboeva ◽  
E. Y. Zakharova ◽  
E. A. Nikolaeva ◽  
I. V. Kanivets ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Hunter Syndrome ◽  
Syndrome Type ◽  
Type Ii
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