Primordial dwarfism and slender bone disorder
MONDO:0800063A skeletal dysplsia characterized by primordial dwarfism, an extreme growth deficiency disorder that has its onset during embryonic development and persists throughout life and slender bone disorder, a heterogeneous group of neonatal dwarfism syndromes, usually of unknown etiology, associated with gracile (thin) bones, multiple fractures, and prenatal or early postnatal death.
9 clinical trials for this condition and its sub-types, 0 tagged with Primordial dwarfism and slender bone disorder itself.
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Sub-types of Primordial dwarfism and slender bone disorder
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IMAGe syndrome 5 trials
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Kenny-Caffey syndrome 0 trials · 4 incl. sub-types
2 sub-types
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Lowry-Wood syndrome 1 trial
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Roifman syndrome 1 trial
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Microcephalic osteodysplastic primordial dwarfism types I and III 0 trials · 1 incl. sub-types
2 sub-types
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3M syndrome 1 0 trials
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3M syndrome 2 0 trials
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3M syndrome 3 0 trials
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Hallermann-Streiff syndrome 0 trials
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Rothmund-Thomson syndrome type 3 0 trials
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Seckel syndrome 10 0 trials
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Seckel syndrome 2 0 trials
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Seckel syndrome 5 0 trials
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Seckel syndrome 8 0 trials
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Seckel syndrome 9 0 trials
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1 sub-type
- Bilateral generalized polymicrogyria 0 trials
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Osteocraniostenosis 0 trials