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Helmut Weyers
German paediatrician and paedontologist, 1920-1986. Stade.
Associated eponyms:
Hertwig-Weyers syndrome
Oligodaktyly syndrome
Meyer-Schwickerath and Weyers syndrome
A syndrome marked mainly by ocular abnormalities, craniofacial dysmorphism, dental defects, hand and foot malformations, various skeletal defects, and mildly delayed mental development.
Nager-de Reynier syndrome
A rare syndrome combining the features of mandibulofacial dysostosis with limb abnormalities and other defects.
Weyers' syndrome I
A congenital malformation syndrome with partial or complete atresia of several parts of the gastrointestinal system as well as displacement of the biliary ducts and displacement and obstruction of the adjoining vessels.
Weyers' syndrome II
A syndrome of multiple anomalies of hands, feet, and face, and mild shortness of stature.
Weyers' syndrome IV
A congenital syndrome of abnormalities of the iris
microdontia, oligodontia, enamel hypoplasia, and virilisation. Later, dwarfism and myotonic dystrophy become evident.
Weyers-Fülling syndrome
An ectodermal dysplasia combining multiple oculodentofacial abnormalities due to unknown embryonal damage.
Weyers-Thier syndrome
A symptom complex in the same group as Goldehaar syndrome, Aicardi's syndrome and Jarcho-Levin spondylocostal dysplasia.
Biography:
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