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Maurice Emile Joseph Lamy
French physician and geneticist, 1895-1975.
Associated eponyms:
Debré-Lamy-Lyell syndrome
A rare syndrome characterized by a severe bullous eruption of the skin and mucous membranes, fever, malaise, conjunctivitis, and a diffuse erythema.
Lamy, Mayer and Rathéry theory
A theory of renal secretion.
Lamy-Maroteaux syndrome
A syndrome characterised by prenatal micromelic dwarfism, progressive kyphoscoliosis, multiple joint contractures, etc.
Léri-Weill syndrome
A skeletal dysplasia combining dorsal subluxation of the distal end of the ulna (Madelung deformity) with mesomelic short stature.
Maroeteaux-Lamy syndrome I
An uncommon disorder of mucopolysaccharide marked by dwarfism, hearing loss, and progressive skeletal deformity, etc.
Maroteaux-Lamy syndrome II
A familial form of idiopathic osteolysis.
Maroteaux-Lamy syndrome III
A congenital disease of bone characterized by short-limbed dwarfism, a large skull with persistent fontanelle, and other anomalies.
Maroteaux-Lamy syndrome IV
A familial type of bone dysplasia with the principal symptoms ofshort-trunk dwarfism, back pain, pain in the hips, and limitation of joint movement.
Biography:
Maurice Emile Joseph Lamy commenced his medical career at the hospital for sick children in Paris, the Hôpital des Enfants Malades. His interest soon turned to inherited disorders, and as early as in 1943 he gave an account of the applications of genetics to medicine. Collaborating with Weil, Jean de Grouchy and Pierre Maroteaux, he studied congenital haemolytic anaemias, chromosomal aberrations and mucopolysaccharidosis.
Lamy obtained his medical doctorate in Paris in 1925. In 1950 he was appointed the first ever professor of medical genetics, and he subsequently established a research centre which gained an international reputation. When he retired in 1967, he was succeeded by his long-time collaborator Maroteaux. Lamy was organiser and president of the Fourth International Congress of Human Genetics which was held in Paris in 1971.
Obituary in La nouvelle presse médicale. Paris, 1975, 4: 2894.
We thank Søren Nørby, Copenhagen, Denmark, for information submitted.
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