Dorra Bousnina

Unusual feature of pycnodysostosis: pectus carinatum.

Faten Tinsa, Samia Hamouda, Manel Bellalah, Dorra Bousnina et autres

[Laryngotracheobronchial foreign body in children: predictive factors of respiratory sequelae].

Faten Tinsa, Salem Yahyaoui, Mohamed Jallouli, Dorra Bousnina et autres

BACKGROUND: Inhalation of laryngotracheobronchial foreign body in children is a serious accident that may compromise the prognosis of the child and the respiratory function in the long term. AIM: identify the predictive factors of respiratory sequelae of laryngotracheobronchial foreign body inhalation. METHODS: …

fr (code pays fourni par la source)

INFECTION NÉONATALE ET MÉNINGITE À PNEUMOCOQUE

Faten Tinsa, S. Yahyaoui, Dorra Bousnina, Inès Brini et autres

[Community acquired pneumonia in children].

Faten Tinsa, Khadija Boussetta, Ahmed Gharbi, Dorra Bousnina et autres

BACKGROUND: Community acquired pneumonia is responsible for a high morbidity in children. The etiological diagnosis is not always easy and treatment remains probabilistic. AIM: To analysis clinical patterns and the outcome of community acquired pneumonia and to find arguments in favour of …

fr (code pays fourni par la source)

Infantile onset of Cockayne syndrome without photosensitivity in a Tunisian girl.

Faten Tinsa, Manel Bellalah, Inès Brini, Dorra Bousnina et autres

BACKGROUND: Cockayne syndrome is a rare autosomal recessive disorder with dwarfism, mental retardation, and otherwise clinically heterogeneous features. Classically, the onset of Cockayne syndrome starts in the second year of life. The failure of RNA synthesis to recover to normal rates after …

Tunisie (code pays fourni par la source)

Nodular regenerative hyperplasia of the liver, coeliac disease and Sjogren's syndrome in a child

Faten Tinsa, Inès Brini, Ahmed El May, Dorra Bousnina et autres

Tunisie (code pays fourni par la source)

Monosomy 10q26-qter and trisomy 11q13-qter as a result ofde novo unbalanced translocation

Faten Tinsa, Y. Chebbi, Mounira Meddeb, Dorra Bousnina et autres

Tunisie (code pays fourni par la source)

An Unusual Homozygous Arylsulfatase: A Pseudodeficiency in a Metachromatic Leukodystrophy Tunisian Patient

Faten Tinsa, Catherine Caillaud, Marie Therese Vanier, Dorra Bousnina et autres

Metachromatic leukodystrophy is an autosomal recessive neurodegenerative lysosomal disease characterized by a deficiency of the lysosomal enzyme arylsulfatase A and the subsequent accumulation of sulfatide in neuronal and visceral tissues. Clinical diagnosis is usually confirmed by in vitro analysis of arylsulfatase A …

us, Tunisie, fr (code pays fourni par la source)

Multiple Congenital Anomalies/Mental Retardation Syndrome With Multiple Circumferential Skin Creases: A New Syndrome?

Faten Tinsa, Khaoula Aissa, Mounira Meddeb, Dorra Bousnina et autres

We describe a combination of multiple congenital anomalies, a severe psychomotor retardation and seizures in a 9-year-old Tunisian boy with circumferential ringed skin creases. He had symmetrical circumferential skin creases on arms, legs, and penis. Craniofacial anomalies included: an elongated face, tight …

Tunisie (code pays fourni par la source)

Late Infantile Neuronal Ceroid Lipofuscinosis in a Tunisian Boy

Faten Tinsa, Catherine Caillaud, Manel Jallouli, Héla Louati et autres

The classical form of late infantile neuronal ceroid lipofuscinosis is a childhood hereditary neurodegenerative disease usually fatal in the first decade of life. We report a two-year-old Tunisian boy who presented this form of ceroid lipofuscinosis. A febrile seizure was the presenting …

Tunisie, fr (code pays fourni par la source)

À propos d’un cas de tératome médiastinal rompu dans le poumon

Khédija Boussetta, Fatima Jaziri, Dorra Bousnina, Noureddine Aloui et autres

fr, Tunisie (code pays fourni par la source)