Antimongolism Syndrome (Chromosome 21 Partial Deletion Syndrome; Monosomy 21 Partial Syndrome; G-Deletion Syndrome) 333d32d 333d32d 333d32d 333d32d 333d32d 333d32d
General: Partial monosomy of chromosome 21 with absence of the short arm and part of the long arm of this chromosome.
Ocular: Antimongoloid slant of lid fissures; blepharochalasis; sclerocornea.
Clinical: Hypertony; large ear lobes; prominent nasal bridge; mental retardation; pyloric stenosis; dystrophic nails; retarded growth; heart disease; hemivertebrae; micrognathia.
Collins JF. Handbook of Clinical Ophthalmology.
Doane JF, et al. Bilateral penetrating keratoplasty for sclerocornea in an infant with monosomy 21. Case report and review of the literature. Cornea 1994; 13:454-458.
Lejeune J, et al. Monosomie Partielle Pour un Petit Acrocentrique. C R
Acad Sci (
Magalini SI, Scrascia E. Dictionary
of Medical Syndromes, 2nd ed.
Penrose LS. Antimongolism [Letter]. Lancet
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