The concept of catatonia was formulated in the 1860s by Karl Ludwig Kahlbaum. He coined and gave the name catatonia to the syndromic entity in which the mood symptoms (depression and mania) were primary, and motor symptoms (mutism, negativism, stereotypies, catalepsy and verbigeration) the most characteristic. Although the name has remained stable, this concept has changed in the last century concerning the details of its definition until the current integrative approach in DSM 5. Catatonic phenomena are main components of the 'motor abnormalities' domain in psychiatric, neurologic and general medical disorders and they have to be evaluated in the context of a full psychopatological and neurological examination. In this article, we make a review about clinical and diagnostic issues in catatonia. Catatonic phenomena comprise both state and trait characteristics and have prognostic validity in psychosis. Moreover, providing that motor abnormalities are closer to neurobiological underpinnings than other psychotic symptoms (e.g., positive symptoms of schizophrenia), catatonic phenomena should be studied specifically as targets for neurobiological research.
KEYWORDS:The concept of catatonia was formulated in the 1860s by the German psychiatrist Karl Ludwig Kahlbaum, who gave the name to the clinical entity and published the monograph entitled Die katatonie oder das Spannungsirresein [1]. He was influenced by the description of transient psychotic disorders of French alienists, and mainly by the 'melancholia attonita' described by François Baillarger [2]. Kahlbaum stressed the dominance of abnormal motility over melancholia in the catatonia concept. Thus, he described catatonia as a syndrome in which the mood symptoms (depression and mania) were primary and motor symptoms (mutism, negativism, stereotypies catalepsy and verbigeration) the most characteristic.Motor abnormalities (MAs) are prevalent features in the set of clinical features of psychiatric, neurological and other general medical diseases and these abnormalities are core symptoms of psychotic syndrome [3,4]. They comprise a broad set of symptoms that grouped under different labels have been alleged to be different neurobiological domains, such as catatonic symptoms and signs, extrapyramidal signs and neurological soft and hard signs. Definitions of symptoms related to potential neuromotor domains led to an overlap of terms and different usage across medical disciplines with most neuromotor domains being main symptoms and signs in neurology while catatonic symptoms were relegated to psychiatry. This terminological dichotomy hindered progress in solving the conflict of paradigms in the motor disorders of severe psychiatric illness [5]. In addition, a wide misconception over the years was the reductionism of catatonia and catatonic symptoms to symptoms evidenced in classic descriptions of psychoses nonspecifically related to the pathophysiology of Future Neurol. (Epub ahead of print)