Indian Journal of Ophthalmology

: 1991  |  Volume : 39  |  Issue : 2  |  Page : 68--69

Self-inflicted corneal injuries in a child with congenital sensory neuropathy (A case report)

CH Gaonker1, AK Mukherjee1, SY Gawns2,  
1 Department of Ophthalmology, Goad Medical College, Panaji, Goa 403 001, India
2 Department of Pediatrics, Goad Medical College, Panaji, Goa-403 001, India

Correspondence Address:
C H Gaonker
1133. Kindle. Canacona, Goa - 403 702


An interesting clinical, report of a rare case of bilateral congeni�tal corneal anaesthesia associated with Congenital Sensory Neuropathy (CSN) in a 11sub/2 year old child with corneal ulceration secondary to self-inflicted trauma is reported.

How to cite this article:
Gaonker C H, Mukherjee A K, Gawns S Y. Self-inflicted corneal injuries in a child with congenital sensory neuropathy (A case report).Indian J Ophthalmol 1991;39:68-69

How to cite this URL:
Gaonker C H, Mukherjee A K, Gawns S Y. Self-inflicted corneal injuries in a child with congenital sensory neuropathy (A case report). Indian J Ophthalmol [serial online] 1991 [cited 2023 Jun 10 ];39:68-69
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Self-inflicted eye injuries are a recognised ophthalmic problem in adults with psychological disorders [1],[2];drug addicts [3] and servicemen wishing to avoid military duty . It is also reported in blind children who rub their eyes to obtain vicarious light sensations from mechanical phos�phenes [5]. Corneal ulceration is a recognised complicati�on of congenital corneal anaesthesia , and self-inflicted corneal abrasions have been considered as a cause of intractable corneal ulcers in infants with congenital cor�neal anaesthesia [5]. We report here a case of CSN with bilateral congenital corneal anaesthesia, who came to us with corneal ulceration apparently related to self-in�flicted trauma, the evidence of which was also present elsewhere on the body. The purpose of this communica�tion is to emphasize the role of self-inflicted injuries in the formation of ulcers involving such anaesthetic cor�neas and, to highlight the correlation between congenital corneal anaesthesia and Congenital Sensory Neuropat�hy (CSN), a rare form of Hereditary Sensory Neuropathy in children. This relationship, to our knowledge has not been discussed in previous ophthalmic literature.


A 18 month old female child was observed with a corneal ulcer in the right eye and abrasion of the left cornea. Prior to this, the child had been treated symptomatically for recurrent corneal abrasions on more than two occasio�ns. The parents complained that the child was habitually introducing her fingers in both the eyes since birth. She also had the tendency to bite her lips and fingers and bang the forehead against the wall. Detailed history did not reveal any episodes of fever, convulsions, hyper or anhidrosis, difficulties in swallowing and instability of temperature control. Antenatal history was uneventful and the child was a product of a consanguinous mar�riage, born with no congenital defects.

On ocular examination, there was a corneal ulcer in the inferonasal quadrant of the right eye, approximately 3mm. X 3mm. in size. with mild sions of inflammation.

This was accompanied by an abrasion involving the lower one third of the left cornea. In addition, both corneas showed few macular grade opacities. Corneal sensitivity was tested by the conventional method of moving a wisp of cotton from the limbus towards the centre of the cornea while monitoring for a blink reflex, and was found to be absent in both the eyes (pho�tograph). An accurate and elaborate measurement of the tear secretions was not possible due to poor and inconsistent cooperation of the patient for Schirmer's test. However, an approximate assessment indicating normal tear secretion could be made. The test, done with a 5 mm. X 35 mm. filter paper showed a reading of 18 mm. in the RE and 25 mm. in the LE; the child was crying while the test was being performed in the LE. There were no other abnormal ocular findings.

General examination revealed traumatic amputation of the tip of the tongue and the central portion of the lower lip. Cicatrizing scars were evident at these sites. Both index fingers carried scars of self-mutilation. Detailed neurological and developmental assessment carried out at the paediatric clinic showed that the response to pain was uniformly absent all over the body. The tempera�ture (hot) and touch sensations were affected to a lesser extent. Intellectual development was normal. Tendon reflexes were absent. Careful systemic examination detected no associated anomalies.

Bacterial and fungal tests and conjunctival scrapings from the eyes isolated no pathogens. Haematological and biochemical investigations including serum Vit. A. and serum uric acid were normal. Intradermal histamine test showed positive wheal and flare response. X-ray skull showed thickening of the frontal bone - a feature due to repeated trauma. X-ray chest and cranial ultra�sound were within normal limits.

The corneal ulcer in the RE was treated with topical chloramphenicol and mydriatics and chloramphenicol ointment was used in the LE. Pads were applied con�tinuously to both eyes. The child was placed in arm splints - a measure taken to prevent rubbing of the eyes. With these combined measures, the corneal ulcer hea�led within a few days, leaving a small opacity.


Hereditary Sensory Neuropathy, a group of disorders representing disturbances of sensations, include dif�ferent clinical entities [7],[8]. CSN, transmitted by autosomal recessive inheritance is classified under type II Hereditary Sensory Neuropathy [7] and is characterized by `congenital absence of pain[8]. Some children with features of this disorder are described to have retinitis pigmentosa and the early onset of cataract[8]sub. Corneal anaesthesia described in this report is probably a com�ponent of the universal absence of pain in CSN. Con�genital corneal anaesthesia is also reported in associ�ation with Riley-Day syndrome (Familial Dysautonomia - a type II Hereditary Sensory Neuropathy) [9]; and con�genital insensitivity (indifference) to pain [8],[10] - a disorder known to coexist with Hereditary Sensory Neuropathy[8]. The normal tear secretion and positive flare response to the intradermal histamine test in the absence of other characteristic clinical signs of autonomic dysfunction in our patient, militated against the diagnosis of Riley-Day syndrome.

Cases of isolated congenital anaesthesia have been reported [5],[11] They may also be associated with obvious maldevelopment of the face and skull in Goldenhar syndrome [12].Functional corneal anaesthesia is reported to occur in keratitis artefacta[12]. Severe and generalized self-mutilation in children has been described in Lesch�Nyhan syndrome characterized by convulsions in more than 50% of patients and elevated serum uric acid levels [13]. Moreover, the presence of congenital corneal anaesthesia is not a feature of self-mutilation associated with Lesch-Nyhan syndrome, the Cornelia de Lange syndrome, and the Gilles de la Tourtte syndrome [5].

Irrespective of the theoretical considerations, the self�inflicted corneal abrasions have been accepted as the presenting feature of corneal anaesthesia [5]. Our patient was certainly putting the fingers in her eyes and scratch�ing the eyelids. Both eyes had multiple minor corneal opacities. Furthermore, the observation that the applica�tion of arm splints enhances rapid healing of the corneal ulcers [5], confirms the role of self-inflicted injuries in the causation of intractable ulcerations of the cornea. It is also apparent that the absence of pain was a protective measure against injury which resulted in the mutilation of fingers, lower lip and the tongue secondary to self-in�flicted trauma, forming the presenting feature of CSN.


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