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1.
Rev. Soc. Bras. Med. Trop ; 49(5): 656-659, Sept.-Oct. 2016. tab, graf
Article in English | LILACS | ID: lil-798125

ABSTRACT

Abstract Dengue infection can have spectrum of manifestations, often with an unpredictable clinical progression and outcome. There have been increasing reports of atypical manifestations. Abdominal pain or tenderness and persistent vomiting (warning signs) are present in the majority of cases with severe dengue prior to clinical deterioration. We report a 10-year-old child who presented with fever, persistent vomiting, and abdominal pain. A diagnosis of acute pancreatitis was made. This is a very infrequently reported complication of dengue hemorrhagic fever.


Subject(s)
Humans , Female , Child , Pancreatitis/etiology , Severe Dengue/complications , Pancreatitis/diagnosis , Acute Disease , Severe Dengue/diagnosis
2.
Indian J Hum Genet ; 2013 July-Sept ;19 (3): 363-365
Article in English | IMSEAR | ID: sea-156595

ABSTRACT

Congenital hypoparathyroidism, growth retardation and facial dysmorphism is a rare autosomal recessive disorder seen among children born to consanguineous couple of Arab ethnicity. This syndrome is commonly known as Sanjad- Sakati or hypoparathyroidism‑retardation‑dysmorphism syndrome (HRD). We report 13‑year‑old Hindu boy with hypoparathyroidism, tetany, facial dysmorphism and developmental delay, compatible with HRD syndrome.


Subject(s)
Abnormalities, Multiple/epidemiology , Abnormalities, Multiple/genetics , Adolescent , Adult , Consanguinity , Female , Growth Disorders/epidemiology , Growth Disorders/genetics , Humans , Male , Hypoparathyroidism/epidemiology , Hypoparathyroidism/genetics , Intellectual Disability/epidemiology , Intellectual Disability/genetics , Middle Aged , Osteochondrodysplasias/epidemiology , Osteochondrodysplasias/genetics , Parents , Seizures/epidemiology , Seizures/genetics
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