scholarly journals Dandy-Walker Malformation With Postaxial Polydactyly: Newborn Case Report

Author(s):  
Mustafa ÖZDEMİR ◽  
Tugay TEPE ◽  
Şerif HAMİTOĞLU ◽  
Ahmet İbrahim KURTOĞLU ◽  
Ferda ÖZLÜ ◽  
...  
Author(s):  
Francisco Cammarata-Scalisi ◽  
Colin Eric Willoughby ◽  
María Angelina Lacruz- Rengel ◽  
Enrico Silvio Bertini ◽  
Michele Callea

AbstractPierquin syndrome is a rare genetic entity characterized by the association of Dandy–Walker malformation and postaxial polydactyly. The incidence is uncertain with only six cases previously reported in the literature. In this study, we reported a new case of Pierquin syndrome born from consanguineous parents, characterized by Dandy–Walker malformation, postaxial polydactyly, and congenital heart disease. The case reinforces an autosomal recessive modality of inheritance and expands the phenotypic spectrum of this rare malformation syndrome.


2004 ◽  
Vol 24 (10) ◽  
pp. 796-798 ◽  
Author(s):  
K. L. Deurloo ◽  
J. M. Cobben ◽  
Y. M. Heins ◽  
M. de Ru ◽  
L. C. D. Wijnaendts ◽  
...  

2018 ◽  
Vol 11 (1) ◽  
pp. e226281
Author(s):  
Rajesh Rajput ◽  
Sanat Mishra ◽  
Parul Ahlawat ◽  
Pawan Kumar Yadav

Precocious puberty is characterised by premature appearance of secondary sexual characteristics before the age of 7 years in girls and 9 years in boys. Dandy-Walker malformation comprises a spectrum of intracranial malformations of the posterior fossa. We present a case of a 7-year-old male child who has presented with features of central precocious puberty and on further evaluation has been found to have Dandy-Walker variant and secondary hypothyroidism. The following case report describes this association which is extremely rare and has never been described in literature.


2018 ◽  
Vol 3 (3) ◽  
pp. S26-S27
Author(s):  
Rohit Kapoor ◽  
Neha Rastogi ◽  
Dhwanee Thakkar ◽  
Goutomi Chatterjee ◽  
Anil Sharma ◽  
...  

2019 ◽  
Vol 14 (3) ◽  
pp. 415-418 ◽  
Author(s):  
Alessio Pirino ◽  
Maria Alessandra Sotgiu ◽  
Erich Cosmi ◽  
Andrea Montella ◽  
Pasquale Bandiera

2003 ◽  
Vol 6 (4) ◽  
pp. 355-360 ◽  
Author(s):  
Komala Pillay ◽  
Louise S. Matthews ◽  
Helen C. Wainwright

Extreme variability of expression is characteristic of the facio-auriculo-vertebral sequence. Sporadic and familial cases have been reported with obvious etiologic heterogeneity. Most reports in the literature are of clinical cases. The purpose of this paper is to present a fetal autopsy case report of the facio-auriculo-vertebral sequence in association with DiGeorge sequence, Rokitansky sequence, and Dandy-Walker malformation. A standard neonatal autopsy was performed on a macerated female fetus, gestational age 29 wk. External examination of the fetus revealed hypoplastic right face, low-set microtic right ear, and macrostomia. Internal examination showed hypoplastic thymus and lungs, a type I truncus arteriosus, and ventricular septal defect. Both kidneys showed evidence of pelvi-ureteric junction obstruction. The ovaries and fallopian tubes were present with an absent uterus and vagina (Rokitansky sequence). In addition, Dandy-Walker malformation was identified. Microscopically, a single hypoplastic parathyroid gland was noted and there was cystic renal dysplasia. We report the sixth case of the facio-auriculo-vertebral sequence in association with Rokitansky sequence and the first case of this sequence in association with Dandy-Walker malformation. In addition, features of DiGeorge sequence were present.


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