Cure My Disease

Don't miss your cure!

 Log in / Sign up

Primordial dwarfism and slender bone disorder

MONDO:0800063

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.

43 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Autosomal recessive Kenny-Caffey syndrome (4) IMAGe syndrome (4) Lowry-Wood syndrome (1) Microcephalic osteodysplastic dysplasia, Saul-Wilson type (1) Microcephalic osteodysplastic primordial dwarfism type I (1) Microcephalic osteodysplastic primordial dwarfism type II (1) Roifman syndrome (1) 3M syndrome 1 (0) 3M syndrome 2 (0) 3M syndrome 3 (0) Autosomal dominant Kenny-Caffey syndrome (0) Bilateral generalized polymicrogyria (0) Hallermann-Streiff syndrome (0) Hypoparathyroidism-retardation-dysmorphism syndrome (0) Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency (0) Kenny-Caffey syndrome (0) Microcephalic osteodysplastic primordial dwarfism, type 3 (0) Microcephalic osteodysplastic primordial dwarfism types I and III (0) Microcephalic primordial dwarfism, Alazami type (0) Microcephalic primordial dwarfism due to RTTN deficiency (0)

Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Bone disorder (47) Human disease (14) Skeletal system disorder (4) Disease of genetic or genomic mechanism (2) Skeletal dysplasia (1) Disease by body system or component (0) Disease by etiologic mechanism (0)
Trials to join now! 23 Not yet recruiting 6 Not yet finished but already full! 4 Completed 8 Terminated 2
Sort by