Orthotopic liver transplantation for acute liver failure secondary to autoimmune hepatitis in a child with autoimmune polyglandular syndrome type 1

2002 ◽  
Vol 6 (2) ◽  
pp. 166-170 ◽  
Author(s):  
Dominic Smith ◽  
Mark D. Stringer ◽  
Judy Wyatt ◽  
Moira O'Meara ◽  
Suzanne Davison ◽  
...  
1998 ◽  
Vol 28 ◽  
pp. 226
Author(s):  
P. Obermayer-Straub ◽  
S. Braun ◽  
S. Loges ◽  
M.G. Clemente ◽  
B. Lüttig ◽  
...  

Author(s):  
S. T. Binoj ◽  
Johns Shaji Mathew ◽  
M. Abdul Razak ◽  
Krishnanunni Nair ◽  
Shweta Mallick ◽  
...  

Author(s):  
Ifeanyi Nwosu ◽  
Oreoluwa Oladiran ◽  
Chinyere Ogbonna-Nwosu ◽  
Anulika Anyata

2004 ◽  
Vol 36 (8) ◽  
pp. 2228-2229 ◽  
Author(s):  
D.S. Lee ◽  
J.G. Woo ◽  
H.H. Lee ◽  
K.W. Lee ◽  
J.W. Joh ◽  
...  

2021 ◽  
Vol 14 (4) ◽  
pp. e241680
Author(s):  
Aditya Sanjeevi ◽  
Adlyne Reena Asirvatham ◽  
Karthik Balachandran ◽  
Shriraam Mahadevan

A 45-year-old woman presented to us with a short-term history of nausea, vomiting and giddiness. On arrival at our hospital, examination revealed postural hypotension. Fluid resuscitation with intravenous normal saline was commenced. She also had chronic mucocutaneous candidiasis and nail changes suggestive of ectodermal dystrophy. Detailed history taking revealed that she had never attained menarche. Serum biochemistries showed hyponatraemia, hyperkalaemia, and hypocalcaemia (sodium, 127 mEq/L; potassium, 6 mEq/L; and albumin-corrected calcium, 6 mg/dL). Adrenocorticotropic hormone-stimulated cortisol (16.7 mcg/dL) was suboptimal favouring adrenal insufficiency. She was started on hydrocortisone and fludrocortisone supplementation. Additionally, the parathyroid hormone was inappropriately low (3.8 pg/mL) confirming hypoparathyroidism. Oral calcium and active vitamin D supplementation were added. With the above clinical and biochemical picture, namely, clustering of primary amenorrhoea, adrenal insufficiency and hypoparathyroidism, the diagnosis pointed towards autoimmune polyglandular syndrome. Genetic workup revealed a deletion in exon 8 of the autoimmune regulator gene confirming the diagnosis of autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy/autoimmune polyglandular syndrome type 1 .


2002 ◽  
Vol 15 (7) ◽  
pp. 369-373 ◽  
Author(s):  
Sanjiv Saigal ◽  
Parthi Srinivasan ◽  
John Devlin ◽  
Bastiaan Boer ◽  
Buxton Thomas ◽  
...  

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