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Primordial dwarfism and slender bone disorder

A 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.

0 trials tagged with this condition →

IMAGe syndrome 5 trials
Kenny-Caffey syndrome 0 trials · 4 incl. sub-types Sub-types →
Lowry-Wood syndrome 1 trial
Roifman syndrome 1 trial
Microcephalic osteodysplastic dysplasia, Saul-Wilson type 1 trial
Microcephalic osteodysplastic primordial dwarfism type II 1 trial
Microcephalic osteodysplastic primordial dwarfism types I and III 0 trials · 1 incl. sub-types Sub-types →
3M syndrome 1 0 trials
3M syndrome 2 0 trials
3M syndrome 3 0 trials
Hallermann-Streiff syndrome 0 trials
Rothmund-Thomson syndrome type 3 0 trials
Seckel syndrome 10 0 trials
Seckel syndrome 2 0 trials
Seckel syndrome 5 0 trials
Seckel syndrome 8 0 trials
Seckel syndrome 9 0 trials
Hypoparathyroidism-retardation-dysmorphism syndrome 0 trials
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency 0 trials
Microcephalic primordial dwarfism due to RTTN deficiency 0 trials Sub-types →
Microcephalic primordial dwarfism, Alazami type 0 trials
Microcephalic primordial dwarfism, Toriello type 0 trials
Microcephaly 13, primary, autosomal recessive 0 trials
Osteocraniostenosis 0 trials
Short stature, microcephaly, and endocrine dysfunction 0 trials
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome 0 trials