Moritz Heinrich Romberg

Moritz Heinrich Romberg (1795-1873)

Moritz Heinrich Romberg (1795-1873) was a German neurologist.

Leading German neurologist of the nineteenth century and the author of the first modern classification of neurological disorders – Lehrbuch der Nervenkrankheiten des Menschen, published in three volumes between 1840 and 1846. Sieveking translated into English in 1853 [A manual of the nervous diseases of man].

Romberg described the physiology of neurological function and constructed a now outdated nosology of nervous system disorders, the first real attempt to systematise neurological disease.

Remembered for the neurological sign related to involvement of the dorsal column of the spinal cord in patients with tabes dorsalis (Romberg sign); progressive facial hemiatrophy (Parry-Romberg syndrome); and obturator hernia incarceration (Howship-Romberg sign)


  • Born 11th November 1795 Meiningen (Thüringen)
  • 1817 – MD, University of Berlin – Thesis on ‘congenital rickets’ with comprehensive description of achondroplasia.
  • 1820 – Postgraduate training in Vienna with Johann Peter Frank (1745 – 1821). Frank was a German physician and public health pioneer recognised for his contributions in spinal cord disease and was responsible for directing Romberg’s career towards neurology.
  • 1821 – Physician to the poor, Berlin. He held this role for 25 years.
  • 1830 – Appointed Privatdozent of special pathology and therapy at the University of Berlin.
  • 1831 and 1837 – Director of the cholera hospital during the Berlin cholera epidemics.
  • 1838 – Appointed extraordinary professor of pathology at the University of Berlin
  • 1840 – Appointed director of the university hospital
  • 1845 – Chair of Medicine and directorship, the Royal Policlinic Institute at the Friedrich Wilhelm University, Berlin.
  • Died on 16th June 1873, Berlin of heart disease.

Medical Eponyms

Howship-Romberg sign (1840, 1847)

Pain and paraesthesia along the inner (medial) aspect of the thigh, down to the knee; and pain on internal rotation of the hip along the distribution of the obturator nerve. Caused by compression of the obturator nerve most commonly associated with strangulated obturator hernia. Named with English surgeon John Howship (1781 – 1841)

Romberg described his findings of an obturator hernia and their clinical significance in 1847, published in 1848 as ‘Die Operation des eingeklemmten Bruches des eirunden Loches

Romberg summarised the diagnostic criteria for obturator hernia:

Romberg Sign (Romberg test) 1846

Romberg gives a thorough account of the muscular weakness, tabetic gait, urinary frequency, retention and incontinence and the constricting girdle pains associated with tabes dorsalis. In particular he provides an account of sensory ataxia

Early in the disease we find the sense of touch and muscular sense diminished, while the sensibility of the skin is unaltered in reference to temperature and painful impressions. The feet feel numbed in standing, walking or lying down, and the patient has the sensation as if they were covered in fur; the resistance of the ground is not felt …The gait begins to be insecure…he puts down his feet with greater force… The individual keeps his eyes on his feet to prevent his movements from becoming still more unsteady. If he is ordered to close his eyes while in the erect posture, he at once commences to totter and swing from side to side; the insecurity of his gait also exhibits itself more in the dark. It is now ten years since I pointed out this pathognomonic sign, and it is a symptom which I have not observed in other paralyses, nor in uncomplicated amaurosis…in no case have I found it wanting

Romberg 1846; 1: 794-801.

Parry-Romberg syndrome (1825, 1846) (Romberg syndrome)

Parry-Romberg syndrome: rare disorder of progressive facial hemiatrophy. Slowly progressive atrophy of the soft tissues of one side of the face, associated with trigeminal neuralgia and involvement of the eyes and hair. Muscles, cartilage and the underlying bony structures may also be involved.

Key Medical Attributions

In Lehrbuch der Nervenkrankheiten des Menschen 1840-1846 Romberg drew prevailing neurological theories together and presented a systematic and ordered approach to neurology. He combined pathophysiological features with clinical observations and treatment strategies. Of note he dichotomised disorders into ‘Neuroses of Sensibility’ (sensory or afferent disorders) and ‘Neuroses of Motility‘ (motor or efferent disorders).

Romberg gives an unmistakable description of Argyll Robertson pupils prior to the eponymous description by Douglas Argyll Robertson.

Other contributions to medicine span the areas of epilepsy and achondroplasia while further clinical descriptions include pupillary abnormalities in tertiary syphilis and the cremasteric reflex.

I have selected the study of diseases of the nervous system for the object of my life and goal of my researches


Romberg was one of many physicians who incorrectly attributed the discovery of the function of the anterior and posterior roots of the spinal cord to Charles Bell, when in fact the finding was of François Magendie. Not backwards in coming forwards…

Romberg takes a swipe at his erstwhile colleagues in neurology…

The blame lies in a measure with the distinguished members of our profession who have been deterred by a fear that pathological investigations would fail to cope with the advanced state of physiological inquiry; in others, the fault is to be attributed to that mental indolence, which gives the preference to the easy path of tradition, and with foolish scepticism rejects everything that is new.

Romberg MH, 1840

Major Publications

Romberg translated two seminal neurology texts into German:


eponymictionary CTA


the person behind the name

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