Author(s)

Mariem Labrahimi^*, Madiha Benhachem, Aziza Elouali, Ayad Ghanam, Maria Rkain, Abdeladim Babakhouya

Department of Pediatrics, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed Premier, Oujda, Morocco.

Hennekam syndrome is a rare autosomal recessive disorder that was first described in 1989. It is characterized by congenital lymphoedema of the limbs, genitals, and face; intestinal lymphangiectasia; variable mental retardation; and typical craniofacial dysmorphism. The syndrome is genetically heterogeneous, which explains the variability of the clinical phenotype. We present a case report of a 16-month-old male infant who was born to consanguineous parents. The infant exhibited generalized lymphoedema, typical dysmorphic facial features, psychomotor development retardation, and respiratory distress due to upper airway obstruction caused by the absence of the lingual frenulum. To our knowledge, this anomaly has not been previously reported in the literature.

Lymphangiectasia, Lymphoedema, Hennekam Syndrome

Labrahimi, M. , Benhachem, M. , Elouali, A. , Ghanam, A. , Rkain, M. and Babakhouya, A. (2023) Hennekam Syndrome: A Case Report. Open Access Library Journal, 10, 1-4. doi: 10.4236/oalib.1110168.