scholarly journals VP36.05: A rare syndrome with a rare association: Dandy‐Walker associated with an occipital meningocele

2021 ◽  
Vol 58 (S1) ◽  
pp. 251-251
Author(s):  
G. Berraies ◽  
M. Garci ◽  
S. Armi ◽  
C. Belghith ◽  
T. Makhlouf ◽  
...  
Keyword(s):  
Rare Association ◽  
Rare Syndrome

scholarly journals Vascular Malformation and Common Keratinocytic Nevus of the Soft Type: Phacomatosis Pigmentovascularis Revisited

2014 ◽  
Vol 2014 ◽  
pp. 1-3 ◽  
Author(s):  
André Laureano ◽  
Rodrigo Carvalho ◽  
Cristina Amaro ◽  
Isabel Freitas ◽  
Jorge Cardoso
Keyword(s):  
Vascular Malformation ◽  
Rare Association ◽  
Rare Syndrome ◽  
Phacomatosis Pigmentovascularis ◽  
Traditional Classification ◽  
Type Ia ◽  
Pigmented Nevus

Phacomatosis pigmentovascularis is a rare syndrome characterized by the coexistence of a pigmented nevus and a cutaneous vascular malformation. We report a 5-year-old boy with all the typical findings of phacomatosis pigmentovascularis type Ia. Although its existence according to the traditional classification has been questioned, this case represents a very rare association of a capillary vascular malformation and a common keratinocytic nevus of the soft type.

Rare association of primary hyperparathyroidism and toxic multinodular goiter

2018 ◽  
Author(s):  
Hamza Elfekih ◽  
Mouna Elleuch ◽  
Dorra Ghorbel ◽  
Faten Hadjkacem ◽  
Mouna Ammar ◽  
...  
Keyword(s):  
Primary Hyperparathyroidism ◽  
Multinodular Goiter ◽  
Rare Association ◽  
Toxic Multinodular Goiter

A rare association of Adrenocortical carcinoma with haematological and breast malignancy in a young female

2019 ◽  
Author(s):  
Muhammad Murtaza Shafqat ◽  
Naveed Khalily ◽  
Herpret Deol ◽  
Aamir Naeem ◽  
Shujah Dar
Keyword(s):  
Adrenocortical Carcinoma ◽  
Young Female ◽  
Rare Association ◽  
Breast Malignancy

A rare association of hypogonadotropic hypogonadism and GH deficiency in a patient with Addison’s disease

2020 ◽  
Author(s):  
Hiba-Allah Chatti ◽  
Ibtissem Oueslati ◽  
Meriem Yazidi ◽  
Nadia Khessairi ◽  
Wafa Grira ◽  
...  
Keyword(s):  
Gh Deficiency ◽  
Hypogonadotropic Hypogonadism ◽  
Addison’S Disease ◽  
Addison's Disease ◽  
Rare Association

A RARE ASSOCIATION OF MORGAGNI HERNIA WITH DOWN SYNDROME.

2016 ◽  
Vol 4 (11) ◽  
pp. 1044-1048
Author(s):  
Kumaraguru. V ◽  
◽  
AshokSwaminathan Govindarajan ◽  
Subramanian C.S ◽  
Prof.T.R.K. Madhavan ◽  
...  
Keyword(s):  
Down Syndrome ◽  
Morgagni Hernia ◽  
Rare Association

scholarly journals A rare association of caecal volvulus and intestinal malrotation causing an acute abdomen: Case report

2021 ◽  
pp. 102357
Author(s):  
Youssef Chaker ◽  
Ouadi Yacine ◽  
Ben Mahmoud Ahmed ◽  
Haddad Anis ◽  
Magherbi Houcine ◽  
...  
Keyword(s):  
Case Report ◽  
Acute Abdomen ◽  
Intestinal Malrotation ◽  
Rare Association
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