This female infant was the 3,200 g product of a 38-week gestation delivered by spontaneous vaginal delivery to a 30-year-old mother. The mother's pregnancy was uncomplicated, and the family history was unremarkable. At birth, the baby was noted to have a prominent forehead, narrow palpebral fissure, hypertelorism, and a broad nose (Fig. 1A). Skeletal survey showed bilateral hypoplastic first ribs, right-sided fifth finger clinodactyly, and prominent long phalanges of the fourth digits on both feet (Fig. 1B and 1C). She was suspected to have a chromosomal anomaly and was referred to the ophthalmology department for evaluation of possible ocular abnormalities. On examination at two weeks of age, she had weak pupillary response to light but no blink or avoidance response to strong light. With regard to the horizontal length of the palpebral fissure, the right and the left were 1.7 and 1.6 cm, respectively, which was considered short. Telecanthus and hypertelorism were also present; intercanthal distance was 2.8 cm, and interpupillary distance was 4.3 cm (Fig. 2). Slit-lamp examination of both eyes revealed normal anterior segments, and dilated fundus examination revealed normal optic nerves and retinal vasculature. Retinal pigment epithelial mottling and atrophy in the macula of both eyes with diffuse retinal pigmented epithelium drop-out in the mid and periphery were observed (Fig. 3). After a three-month lapse from the original examination, fix and follow behavior was not consistent in either eye, and there were no interval changes to the lesions in the retina. Continued observation after this was no longer possible due to follow-up loss.

An echocardiogram demonstrated a small ventricular septal defect and patent ductus arteriosus, and an abdominal ultrasound showed a normal sized liver and kidneys with normal echogenicity. Chromosomal analysis of peripheral blood revealed a mosaic complement with trisomy 14 (47,XX,+14) and a normal female complement (46,XX) (Fig. 4).

Neither parent had a significant past medical history nor a family history of ophthalmologic issues, and both had normal fundus findings. Also, the results of chromosomal analysis were normal in peripheral blood.

Although complete trisomy 14 is not compatible with postnatal life, trisomy 14 mosaicism has been diagnosed in newborns and children with multiple congenital anomalies [1,2]. This chromosomal abnormality was first described in 1970, and there are several characteristic features which may enable the clinician to suspect this diagnosis prior to obtaining a chromosome analysis [1]. The most common features are growth and psychomotor retardation, dysmorphic craniofacial features such as abnormal or low-set ears, micrognathia, cleft or highly arched palate, short neck, and congenital heart and genitourinary abnormalities [2]. Ophthalmologic features include hypo- and hypertelorism, downward slanting of the palpebral fissure, blepharoptosis, deep-set eye, eversion of the eyelids, a "evanescent translucent film over the eyes," and microophthalmia [1-4].

Retinal pigmentary dystrophy was not previously described in any reports of this chromosomal abnormality. In other chromosomal abnormalities such as trisomy 21 (Down's syndrome) and trisomy 18 (Edward's syndrome), retinal pigment epithelium abnormalities are reported to be a clinical feature. In trisomy 21, focal hyperplasia of the retinal pigment epithelium has been reported, and retinal depigmentation is reported to be a clinical feature in trisomy 18 [5,6].

In mosaic trisomy 14, several other more unusual features have been described but are seen in a smaller percentage of patients. One such feature is abnormal skin pigmentation, which is a common finding in individuals with mosaic chromosomal abnormality. In trisomy 14 mosaicism, hyper- and hypopigmentation of the skin have been reported, so chromosome 14 is supposed to be related to pigmentation of the epithelium. The patient we describe did not exhibit abnormal skin pigmentation at birth, yet this was evident by three months [7,8].

Howard et al. [9] have reported a patient who had a ring 14 with a terminal deletion but no retinal pigmentation. They suggested that a region on chromosome 14 proximal to q32.2 might be involved in controlling these changes.

Further electrophysiologic testing would be helpful to determine if there are any abnormalities of either the rods or cones in association with trisomy 14 mosaicism, though neither has been previously reported. Unfortunately, electroretinogram testing was not possible in this patient. Yet, the lesion of the retina persisted for three months; lesions both in the periphery as well as in the posterior pole should be considered as retinal dystrophy. We expand the clinical spectrum of this rare entity with dysmorphic features and ocular abnormalities to include retinal dystrophy.