Faten Tinsa

Summary

Country: France

Publications

  1. doi Atypical teratoid/rhabdoid tumor of the spine in a 4-year-old girl
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Tunis, Tunisia
    J Child Neurol 23:1439-42. 2008
  2. doi Congenital salivary gland anlage tumor of the nasopharynx
    Faten Tinsa
    Children s Hospital of Tunis, Department of Pediatrics B, Tunisia
    Fetal Pediatr Pathol 29:323-9. 2010
  3. doi Abdominal tuberculosis in children
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Tunis, Tunisia
    J Pediatr Gastroenterol Nutr 50:634-8. 2010
  4. doi Central system nervous tuberculosis in infants
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Tunis, Tunisia
    J Child Neurol 25:102-6. 2010
  5. doi Perianal presentation of Langerhans cell histiocytosis in children
    F Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Boulevard 9 avril, 1007 Jabbary, Bab Saadoun, Tunis, Tunisia
    Gastroenterol Clin Biol 34:95-7. 2010
  6. doi Giant condyloma acuminatum in an infant
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Tunis, Tunisia
    Pediatr Dermatol 26:488-9. 2009
  7. doi Monosomy 10q26-qter and trisomy 11q13-qter as a result of de novo unbalanced translocation
    F Tinsa
    Department of Paediatrics B of the Children s Hospital of Tunis, Jabbary, Bab Saadoun, Tunis, Tunisia
    J Appl Genet 50:289-91. 2009
  8. doi An unusual homozygous arylsulfatase: a pseudodeficiency in a metachromatic leukodystrophy Tunisian patient
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Tunis, Tunisie
    J Child Neurol 25:82-6. 2010
  9. doi Megalencephalic leukoencephalopathy with subcortical cysts in a Tunisian boy
    Faten Tinsa
    Department of Pediatrics B of the Children s Hospital of Tunis, Tunis, Tunisia
    J Child Neurol 24:87-9. 2009
  10. doi Multiple congenital anomalies/mental retardation syndrome with multiple circumferential skin creases: a new syndrome?
    Faten Tinsa
    Department of Pediatrics of the Children s Hospital of Tunis, Tunis, Tunisia
    J Child Neurol 24:224-7. 2009

Collaborators

Detail Information

Publications21

  1. doi Atypical teratoid/rhabdoid tumor of the spine in a 4-year-old girl
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Tunis, Tunisia
    J Child Neurol 23:1439-42. 2008
    ..Magnetic resonance imaging The authors showed an intramedullary mass extending from the bulbomedullary junction to T1 with leptomeningeal dissemination. The patient died 2 weeks after diagnosis...
  2. doi Congenital salivary gland anlage tumor of the nasopharynx
    Faten Tinsa
    Children s Hospital of Tunis, Department of Pediatrics B, Tunisia
    Fetal Pediatr Pathol 29:323-9. 2010
    ..The tumor was removed and the outcome was favourable without recurrence at five years of the follow up...
  3. doi Abdominal tuberculosis in children
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Tunis, Tunisia
    J Pediatr Gastroenterol Nutr 50:634-8. 2010
    ..The most common forms of abdominal TB in children are adhesive peritonitis and nodal disease...
  4. doi Central system nervous tuberculosis in infants
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Tunis, Tunisia
    J Child Neurol 25:102-6. 2010
    ..These localizations are very rare. On the follow-up, 3 patients had hypoacousia and only 1 had severe sequelae, despite a diagnostic delay...
  5. doi Perianal presentation of Langerhans cell histiocytosis in children
    F Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Boulevard 9 avril, 1007 Jabbary, Bab Saadoun, Tunis, Tunisia
    Gastroenterol Clin Biol 34:95-7. 2010
    ..Biopsy of the lesions showed Langerhans cell histiocytosis. This patient did not have any other organ involvement, which is rare. The outcome was favourable with vinblastine and corticoids...
  6. doi Giant condyloma acuminatum in an infant
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Tunis, Tunisia
    Pediatr Dermatol 26:488-9. 2009
    ..These lesions were treated by surgical excision with satisfactory results. This size, extent, and early age of appearance make this case highly unusual...
  7. doi Monosomy 10q26-qter and trisomy 11q13-qter as a result of de novo unbalanced translocation
    F Tinsa
    Department of Paediatrics B of the Children s Hospital of Tunis, Jabbary, Bab Saadoun, Tunis, Tunisia
    J Appl Genet 50:289-91. 2009
    ..He had craniofacial dysmorphy, congenital heart defects, urogenital and cerebral anomalies, and severe developmental delay. To the best of our knowledge, this is the first report of this combination of chromosomal abnormalities...
  8. doi An unusual homozygous arylsulfatase: a pseudodeficiency in a metachromatic leukodystrophy Tunisian patient
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Tunis, Tunisie
    J Child Neurol 25:82-6. 2010
    ..This patient was found to be homozygous for the arylsulfatase A pseudodeficiency. This condition is rare and can lead to a severe disease. Prenatal diagnosis was performed in this family, and the fetus was healthy...
  9. doi Megalencephalic leukoencephalopathy with subcortical cysts in a Tunisian boy
    Faten Tinsa
    Department of Pediatrics B of the Children s Hospital of Tunis, Tunis, Tunisia
    J Child Neurol 24:87-9. 2009
    ..The mutation was found to be heterozygous in the parents. To the best of the authors' knowledge, this mutation has never been reported...
  10. doi Multiple congenital anomalies/mental retardation syndrome with multiple circumferential skin creases: a new syndrome?
    Faten Tinsa
    Department of Pediatrics of the Children s Hospital of Tunis, Tunis, Tunisia
    J Child Neurol 24:224-7. 2009
    ..Chromosomal analysis revealed a normal male karyotype with 46,XY. Skin biopsy was normal. To the best of our knowledge, this combination of anomalies has not been reported and this case may be a unique syndrome...
  11. ncbi Infantile onset of Cockayne syndrome without photosensitivity in a Tunisian girl
    Faten Tinsa
    Department of Pediatrics B of the Children s Hospital of Tunis, Tunis, Tunisia
    Tunis Med 87:877-9. 2009
    ..The failure of RNA synthesis to recover to normal rates after UV-C irradiation provides a useful diagnostic test and the clinical feature that correlates most strongly with defective RNA synthesis is photosensitivity...
  12. ncbi Mediastina Tuberculosis mass in a three-month-old boy
    Khadija Boussetta
    Department of Pediatrics B of the Children s Hosptial of Tunis, Tunis, Tunisia
    Tunis Med 88:602-4. 2010
    ..Mediastinal mass of tuberculous origin is exceedingly rare in infant...
  13. ncbi [Community acquired pneumonia in children]
    Faten Tinsa
    Service de m├ędecine infantile B, Hopital d Enfants de Tunis, Tunis, Tunisie
    Tunis Med 87:851-6. 2009
    ..Community acquired pneumonia is responsible for a high morbidity in children. The etiological diagnosis is not always easy and treatment remains probabilistic...
  14. ncbi Marfan syndrome in a Triple-X girl: a new association?
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis
    Tunis Med 88:203-6. 2010
    ..Triple X is a sex chromosomal abnormality that involves the presence of three sex chromosomes resulting in 47, XXX karyotype. Most patients suffering from this syndrome are usually mentally normal or subnormal with no gross malformation...
  15. ncbi Neonatal meningitis by Neisseria meningitidis B
    Faten Tinsa
    Department of Pediatrics of the Children s Hospital of Tunis, Tunis, Tunisia
    Tunis Med 86:1014-5. 2008
    ..Neisseria meningitidis is one of the major causes of meningitis in children and adolescents, but it is uncommonly found in neonatal meningitis...
  16. ncbi Unusual case of thiamine responsive megaloblastic anemia
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis
    Tunis Med 87:159-63. 2009
    ..Thiamine-responsive megaloblastic anemia syndrome is a rare autosomal recessive disorder defined by the occurrence of megaloblastic anemia, diabetes mellitus, and neurosensoriel deafness, responding in varying degrees to thiamine treatment...
  17. ncbi [Role of lumbar puncture for febrile seizure among infants under one year old]
    Faten Tinsa
    Service de m├ędecine infantile B, Hopital d Enfants de Tunis, Place Bab saadoun Jabbary, Tunis, Tunisie
    Tunis Med 88:178-83. 2010
    ..Febrile seizure is a frequent cause of hospitalization. Its management remains problematic. According to the American Academy of Pediatrics, lumbar puncture, which is not devoid of risk, is strongly recommended in infants under 1 year...
  18. ncbi A randomized, controlled trial of nebulized terbutaline for the first acute bronchiolitis in infants less than 12-months-old
    Faten Tinsa
    Department of Pediatrics B of the Children s Hospital of Tunis, Boulevard 9 avril, 1007 Jabbary, Tunis, Tunisia
    Tunis Med 87:200-3. 2009
    ..The aim of this study is to evaluate the efficacy of nebulized terbutaline in bronchiolitis as measured by improvement in clinical score, oxygen saturation or reduction in duration of hospitalization...
  19. ncbi Fanconi anemia complicated by neutropenic enterocolitis
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Tunis, Tunisia
    Tunis Med 86:1011-3. 2008
    ....
  20. ncbi Congenital cutaneous candidiasis associated with respiratory distress in a full-term newborn
    Faten Tinsa
    Department of Pediatrics B, Children s Hospital of Tunis, Tunis, Tunisia
    Tunis Med 88:844-6. 2010
    ..Amphotericin B is the first-line agent for the treatment of systemic disease. Aim: To describe a congenital candidiasis in a full-term newborn...
  21. ncbi Pyelonephritis xanthogranulomatous in childhood: case report and literature review
    Wiem Douira
    Department of Radiology, Children s Hospital, Tunis, Tunisia
    Tunis Med 87:538-41. 2009
    ..Xanthogranulomatous pyelonephritis (XGP) is a specific form of chronic inflammatory kidney disease rarely seen in children. The Symptoms are often vague and non-specific..