Protein-losing gastroenteropathy with facial anomaly and growth retardation: A mild case of Hennekam syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference6 articles.
1. Intestinal lymphangiectasia, lymphedema, mental retardation, and typical face: Confirmation of the Hennekam syndrome
2. (1959) “Radiographic Atlas of Skeletal Development of the Hand and Wrist.” 2nd ed. Stanford: Stanford University Press.
3. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation
4. Protein-Losing Enteropathy in Atopic Dermatitis
5. (1988) “Smith's Recognizable Patterns of Human Malformation.” 4th ed. Philadelphia: WB Saunders, pp 560-561.
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1. A Multiplex Kindred with Hennekam Syndrome due to Homozygosity for a CCBE1 Mutation that does not Prevent Protein Expression;Journal of Clinical Immunology;2015-12-19
2. Variable clinical presentation in primary lymphoedema;Clinical Dysmorphology;2014-07
3. Successful pericardiectomy in Hennekam syndrome;Turkish Journal of Thoracic and Cardiovascular Surgery;2013-10-07
4. Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia;Human Genetics;2009-11-13
5. Hennekam Syndrome Presentıng Wıth Abdomınal Mass;Scottish Medical Journal;2009-08
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