Journal of Medical Genetics · 1991 · 21 citations · 7 references
MedicineEndocrinologyGeneticsHuman GeneticsPediatric EndocrinologyPediatric GeneticsCongenital DisordersCongenital Endocrine DisordersGenetic DisordersGenetic SyndromesGrowth DisordersInherited Endocrine Syndromes3M SyndromeDwarfism SyndromesEndocrine Developmental AnomaliesShort Stature GeneticsSyndromic Craniofacial Disorders
Nine children with primordial dwarfism are described and a new syndrome is delineated. The significant features of this syndrome include facial dysmorphism with gloomy face and very short stature, but no radiological abnormality or hormone deficiency. Mental development is normal. The mode of inheritance seems to be autosomal recessive because of consanguinity in three of the four sibships. Some overlap with the 3-M syndrome is discussed but the autonomy of the gloomy face syndrome seems to be real.
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The 3-M syndrome: a heritable low birthweight dwarfism.
Jordan Miller, V.A. McKusick, P Malvaux et al. · PubMed · 1975 · 74 citations
Medicine, Genetics, Pediatrics +14
Reevaluation of Russell-Silver syndrome
Howard M. Saal, Roberta A Pagon, Melanie Pepin · The Journal of Pediatrics · 1985 · 56 citations
R M Winter, M Baraitser, David Grant et al. · Journal of Medical Genetics · 1984 · 32 citations · Full text
José‐María Cantú · American journal of diseases of children · 1981 · 20 citations
Medicine, Genetics, Pediatrics +16