Rabenhorst cranio-acrofacial syndrome - significado y definición. Qué es Rabenhorst cranio-acrofacial syndrome
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Qué (quién) es Rabenhorst cranio-acrofacial syndrome - definición

RARE CONGENITAL DISORDER
Distal Arthrogryposis, Type IIA; Freeman-sheldon syndrome; Whistling syndrome (Cranio-carpo-tarsal syndrome, Freeman-Sheldon syndrome, Windmill-Vane-hand syndrome, Distal arthrogryposis); Whistling syndrome; Cranio-carpo-tarsal syndrome; Distal arthrogryposis type 2A; Distal arthrogryposis type 2; Windmill–Vane–Hand syndrome; Sheldon-Hall syndrome; Freeman Sheldon Syndrome; Windmill-Vane-Hand syndrome; Freeman-Sheldon syndrome; Freeman-Sheldon

Cranio-corpography         
Cranio-corpo-graphy; Cranio corpography
Cranio-Corpo-Graphy (CCG) is a medical investigation and measurement procedure developed in 1968 by German neurootologist Claus-Frenz Claussen. It documents and evaluates disorders of the equilibrium function measured by investigation procedures such as the Unterberger test, the LOLAVHESLIT test, the NEFERT test, the Romberg's test and the WOFEC test.
Miller syndrome         
HUMAN DISEASE
Genée-Wiedemann syndrome; Wildervanck-Smith syndrome; Genée–Wiedemann syndrome; Miller Syndrome
Miller syndrome, also known as Genée–Wiedemann syndrome, Wildervanck–Smith syndrome or postaxial acrofacial dystosis, is an extremely rare genetic condition that manifests as craniofacial, limb and eye deformities. It is caused by a mutation in the DHODH gene.
Reye's syndrome         
SYNDROME CHARACTERIZED BY ACUTE BRAIN DAMAGE AND LIVER FUNCTION PROBLEMS
Reyes Syndrome; Reye Syndrome; Reye's Syndrome; Reyes syndrome; Reye’s Syndrome; Reye hepatocerebral syndrome; Rye syndrome; Reye s syndrome; Reye's s syndrome; Reye's syndrome; Reye’s syndrome
['re?z, 'r??z]
¦ noun a life-threatening metabolic disorder in young children, of uncertain cause.
Origin
1960s: named after the Australian paediatrician Ralph D. K. Reye.

Wikipedia

Freeman–Sheldon syndrome

Freeman–Sheldon syndrome (FSS) is a very rare form of multiple congenital contracture (MCC) syndromes (arthrogryposes) and is the most severe form of distal arthrogryposis (DA). It was originally described by Ernest Arthur Freeman and Joseph Harold Sheldon in 1938.: 577 

As of 2007, only about 100 cases had been reported in medical literature.