Transient neonatal hypoparathyroidism in two siblings unmasking maternal normocalcemic hyperparathyroidism

2007 ◽  
Vol 167 (4) ◽  
pp. 431-434 ◽  
Author(s):  
Preamrudee Poomthavorn ◽  
Boonsong Ongphiphadhanakul ◽  
Pat Mahachoklertwattana
1992 ◽  
Vol 127 (10) ◽  
pp. 1157 ◽  
Author(s):  
Allan E. Siperstein

2019 ◽  
Vol 12 (8) ◽  
pp. e229160 ◽  
Author(s):  
Pragathi LK ◽  
Raja Kannan P ◽  
Manas Shanbhag

Neonatal hypoparathyroidism is one of the rare causes of hypocalcaemia. Several cases of neonatal hypoparathyroidism secondary to maternal hyperparathyroidism have been reported. In this case report, we have a term neonate with normal birth history who presented with late onset hypocalcemic seizures. After excluding polyendocrinopathies and related syndromes, hypocalcaemia seizures were secondary to maternal asymptomatic hypoparathyroidism. Since this is one variety of unusual case of maternal and fetal hypoparathyroidism, further testing was mandatory to confirm familial origin. This focuses on the need for every clinician to test maternal metabolic status in case of neonatal manifestations.


Endocrine ◽  
2015 ◽  
Vol 50 (3) ◽  
pp. 816-818 ◽  
Author(s):  
Jose Luis Perez Castrillón ◽  
Gonzalo Díaz-Soto ◽  
Olatz Izaola Jauregui ◽  
Enrique Romero ◽  
Daniel de Luis Román

2014 ◽  
Vol 03 (05) ◽  
pp. 253-256 ◽  
Author(s):  
Hemn Muhammed Mustafa ◽  
Mohamed Al Shekhani ◽  
Bnar Jamal

Bone Reports ◽  
2020 ◽  
Vol 13 ◽  
pp. 100703
Author(s):  
Anda Mihaela Naciu ◽  
Gaia Tabacco ◽  
Stefania Falcone ◽  
Assunta Santonati ◽  
Silvia Irina Briganti ◽  
...  

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