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Featured researches published by Reni Ghrahani.


Asia Pacific Allergy | 2014

Age of onset as a risk factor of renal involvement in Henoch-Schönlein purpura

Reni Ghrahani; Masayu Amanda Ledika; Gartika Sapartini; Budi Setiabudiawan

Background Henoch-Schönlein purpura (HSP) is the most common vasculitis in children, characterized by triad of symptoms; palpable purpura without thrombocytopenia, abdominal pain, and arthritis. Renal involvement often occur in children with HSP. No data on the renal involvement of children with HSP in Indonesia, especially West Java. Objective To evaluate renal involvement in children with HSP. Methods Retrospective study was conducted in children with HSP in Department of Child Health, Hasan Sadikin Hospital, from 2006 to 2011. Characteristics and clinical manifestations was reviewed from medical record. HSP was diagnosed by American College of Rheumatology 1990 criteria or European League Against Rheumatism/Pediatric Rheumatology International Trials Organization/Pediatric Rheumatology European Society 2008. Results There were 128 patients, consisting of 82 male (64.9%) and 46 female (35.1%) with ratio 1.8:1. Mean age was 7.9 ± 2.9 years old which range from 6 month to 15 years. Peak morbidity was between 5-10 years old. Prevalence of HSP in Hasan Sadikin Hospital tend to raise from 2.7/100,000 in 2008 to 5.2/100,000 in 2010. In most patients (71%) purpura was the first symptom. Seventy-one patients (44.5%) had arthritis and 89 patients (69.5%) had abdominal pain, while renal involvement was in 28 patients (21.8%). Gastrointestinal manifestations tend to manifest in patients less than 5 years old (p = 0.267), while renal involvement tend to manifest in age group 11-15 years old (p = 0.015) with odds ratio 3.1 (95% confidence interval, 1.2-8.1). Conclusion Renal involvement in children with HSP is more common in age group 11 to 15 years old.


Asia Pacific Allergy | 2011

Vogt-Koyanagi-Harada disease in an 8-year-old boy.

Budi Setiabudiawan; Feti Karfiati; Reni Ghrahani; Gartika Sapartini; Indra Sahril

Vogt-Koyanagi-Harada (VKH) disease is an autoimmune disease involving pigmented tissue in eyes, auditory system, skin, and central nervous system. The pathogenesis is a result of T cell lymphocyte reaction against melanocyte component, tyrosinase and tyrosinase-related protein. This disease uniquely affected pigmented race in Asia and native America, mostly women aged 20-50. We reported an 8-years-old boy complained for visual disturbance since 6 weeks prior admission. Two years earlier, the parents noted the patient eyes were looked red when photographed (suggesting a dilated pupil) preceded by whitened on the right forehead and nose and whitened hair, eyebrow and eyelashes. The examination showed a vitiligo and skin atrophy on right frontal and right nasal, poliosis on the eyebrows, eyelids and hair. The diameter of right pupil was 8 mm, with a paresis on 3rd, 4th, 6th, and 9th nerves. Fundus examination revealed sunset glow appearance. The visual acuity on the right eye: 2/60, left eye: 1-0. Theres positive serology for antitoxoplasma IgG, anti Rubella IgG, anti CMV IgG. The patient was diagnosed with a VKH disease and then prescribed with methylprednisolone 1 mg/kg/day. The patient also had further follow up with dermatovenerologist and ophthalmologist. The eye examination revealed an improvement on right eye panuveitis, with a remaining keratic precipitate in the endothelium, and minimal flare and cell on the anterior chamber. ENT consultation revealed no ear inflammation or hearing disturbance.


Anemia | 2018

Association of Colecalciferol, Ferritin, and Anemia among Pregnant Women: Result from Cohort Study on Vitamin D Status and Its Impact during Pregnancy and Childhood in Indonesia

Raden Tina Dewi Judistiani; Lani Gumilang; Sefita Aryuti Nirmala; Setyorini Irianti; Deni Wirhana; Irman Permana; Liza Sofjan; Hesty Duhita; Lies Ani Tambunan; Jeffry Iman Gurnadi; Umar Seno; Reni Ghrahani; Agnes Rengga Indrati; Yunia Sribudiani; Tetty Yuniati; Budi Setiabudiawan

Studies had shown that iron-cycling was disturbed by inflammatory process through the role of hepcidin. Pregnancy is characterized by shifts of interleukin. Our objective was to determine if 25(OH) vitamin D (colecalciferol) status was associated with ferritin, anemia, and its changes during pregnancy. Method. A cohort study was done in 4 cities in West Java, Indonesia, beginning in July 2016. Subjects were followed up until third trimester. Examinations included were maternal ferritin, colecalciferol, and haemoglobin level. Result. 191 (95.5%) subjects had low colecalciferol, and 151 (75.5%) among them were at deficient state. Anemia is found in 15 (7.5%) subjects, much lower than previous report. Proportion of anemia increased by trimester among women with colecalciferol deficiency. Ferritin status and prepregnancy body mass index in the first trimester were correlated with anemia (r = 0.147, p = 0.038 and r = −0.56, p = 0.03). Anemia in the second trimester was strongly correlated with anemia in the third trimester (r = 0.676, p < 0.01). Conclusion. Our study showed that the state of colecalciferol was not associated with either ferritin state or anemia, but proportion of anemia tends to increase by trimester in the colecalciferol deficient subjects.


Cellular and Molecular Biology | 2018

Fcγ receptor III expression and morphological maturity on neutrophil are associated with higher iron level of major beta-thalassemia

Mohammad Ghozali; Tiwi Harjanti Cakranita; Adi Imam Tjahjadi; Lelani Reniarti; Reni Ghrahani; Mraa. Syamsunarno; Budi Setiabudiawan; Ramdan Panigoro


KnE Life Sciences | 2017

Increased Iron in Pediatric β-Thalassaemia Major Associates with CD3+, Not γδ Lymphocytes

Mohammad Ghozali; Ulrike Panjaitan; Adi Imam Cahyadi Cahyadi; Reni Ghrahani; Lelani Reniarti; Mraa. Syamsunarno; Ramdan Panigoro


Scientific Programming | 2016

Bula Hemoragik dengan Komplikasi Perforasi Gaster Sebagai Manifestasi Klinis Purpura Henoch-Schonlein yang Tidak Biasa pada Anak

Budi Setiabudiawan; Reni Ghrahani; Gartika Sapartini; Nur Melani Sari; Herry Garna


Scientific Programming | 2016

Infeksi Gigi Sebagai Faktor Pencetus Terbanyak Henoch-Schonlein Purpura dengan Keterlibatan Ginjal

Budi Setiabudiawan; Reni Ghrahani; Gartika Sapartini; Minerva Riani Kadir


Paediatrica Indonesiana | 2016

Natural resistance-associated macrophage protein 1 gene polymorphisms in thalassemia patients with tuberculosis infection

Mohammad Ghozali; Sari Puspa Dewi; Reni Ghrahani; Ani Melani Maskoen; Lelani Reniarti; Edhyana Sahiratmadja; Tri Hanggono Achmad


Majalah Kedokteran Bandung | 2015

Pola Antibodi Antinuklear Sebagai Faktor Risiko Keterlibatan Sistem Hematologi Lupus Eritematosus Sistemik pada Anak

Reni Ghrahani; Budi Setiabudiawan; Gartika Sapartini


Majalah Kedokteran Bandung | 2012

Distribusi Subtipe Juvenile Idiopathic Arthritis di Bandung

Reni Ghrahani; Budi Setiabudiawan; Gartika Sapartini; Hesti Puspasari

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Herry Garna

Padjadjaran University

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