Abstracts

CASE REPORT

BARBER-SAY SYNDROME: FURTHER DELINEATION OF THE CLINICAL SPECTRUM

Fanny M. Cortés, Ledia A. Troncoso, Angélica R. Alliende and Bianca L. Curotto

Unidad de Genética y Enfermedades Metabólicas, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, Macul 5540, Santiago, Chile. Send correspondence to F.M.C.

ABSTRACT

We report on a 14-year-old girl who presented a multiple congenital anomaly pattern: ablepharon, hypertelorism, telecanthus, macrostomia, helix agenesis of both ears, redundant thick skin and severe hirsutism, the 5th reported case of Barber-Say syndrome. Our patient had almost the same phenotype as that of the patient cited by Martínez Santana et al. (Am. J. Med. Genet. 47: 20-23, 1993) including the same until then undescribed dermatoglyphic pattern.

INTRODUCTION

In 1982, Barber et al. reported on a 3.5-year-old girl, with a "new" syndrome characterized by ectropion, macrostomia, abnormal skin, severe hypertrichosis, and growth retardation. A second case was reported by David et al. in 1991, with almost the same phenotype, a third case by Martínez Santana et al. (1993), and finally Mazzanti et al. (1998) reported the fourth known case, with the same malformation pattern. Here we report an additional case with exactly the same multiple congenital anomaly pattern.

CASE REPORT

The patient, last of eight otherwise healthy siblings (four boys, four girls), presently 14 years old, was born at term, after the eighth pregnancy of healthy, nonconsanguineous parents (father and mother were 41 and 42 years old, respectively), with no relevant family history. Pregnancy and delivery were normal, with weight of 3400 g, and 50 cm in length at birth. Striking dysmorphic features were immediately noted: ablepharon, hypertelorism, telecanthus, macrostomia, helix agenesis of both ears, redundant thick skin and severe hirsutism especially of the back. No other visceral abnormalities were observed during the neonatal period.

Evaluated at the age of 13 (Figure 1A,B), the patient showed normal mental development. Her anthropometric measurements were: height, 147.5 cm (10th percentile); weight, 37.4 kg (15th percentile), and head circumference, 52.2 cm (40th percentile). Her principal facial features were: aged appearance, ablepharon, ectropion, sparse eyebrows and eyelashes, hypertelorism, telecanthus, bulbous nose with anteverted nares, macrostomia with thin lips, prognatism, abnormally and low set small ears with a prominent antihelix, neither tragus nor lobule, and abnormal external auditory canals which were narrow and tortuous. She had redundant frontal skin and dark thick hair. She had severe hirsutism especially of forehead, neck and back. The thoracic skin was atrophic with hypoplastic nipples. Dermatoglyphic pattern was unusual because no figures except for horizontal ridges in all 10 fingers were present. The rest of the physical examination was within normal limits. Laboratory tests performed included: urine and blood amino acid screening, mucopolysaccharide screening, T3, T4 and TSH, and complete skeletal roentgenograms. All were within normal limits. The banded karyotype was 46,XX.

The patient had normal menses, with menarche at the age of 12. Mental development and neurologic evaluation were completely normal.

DISCUSSION

This study presents the 5th reported case of Barber-Say syndrome. Our patient had almost the same phenotype as that reported by Martínez Santana et al. (1993) including the same until then undescribed dermatoglyphic pattern. Our patient, as the oldest of the five found until now (Table I), provides an opportunity to study phenotype evolution of this disorder with aging, keeping in mind that sexual development was completely normal.

As our patient is the eighth child of healthy non-consanguineous parents and has seven healthy siblings, and based on the nearly identical phenotype described in all reported patients, we assume that this is not a developmental disorder but a genetic condition. Recently, Dinulos and Pagon (1999) reported for the first time a mother to son transmission of this condition, supporting the hypothesis of autosomal dominant inheritance.

While differential diagnosis of this disorder should include ablepharon-macrostomia syndrome (McCarthy and West, 1977; Hornblass and Reifler, 1985, Cesarino et al., 1988), the final diagnosis of Barber-Say in our patient is based on normal development combined with severe hirsutism, not found in the former syndrome. A comparison was made with patients described with associated ablepharon-macrostomia (Table II). Recently, Mazzanti et al. (1998) suggested that Barber-Say and ablepharon-macrostomia syndromes derive from a defective regulation of the same gene.

Both diseases have an apparent sex bias, because in Barber-Say syndrome four of the five patients reported are females and in ablepharon-macrostomia syndrome all patients described are males, but we do not have a clear explanation for this.

The impressive compromise of ectodermal structures in our patient prompted us to consider this disorder an ectodermal dysplasia, as did Martínez Santana et al. (1993) in their paper; unfortunately, our patient and her family refused a skin biopsy.

RESUMO

Apresentamos uma paciente de 14 anos, de sexo feminino, portadora de um quadro de múltiplas anomalias congênitas: hipertelorismo, telecanto, macrostomia, agenesia da hélice em ambos os pavilhões auriculares, pele grossa e redundante e hirsutismo severo, que corresponde ao 5º caso reportado de síndrome de Barber-Say. Esta paciente tem praticamente o mesmo fenótipo que a paciente descrita por Martínez Santana et al. (Am. J. Med. Genet. 47: 20-23, 1992), incluindo o mesmo padrão dermatoglífico que não havia sido descrito até então.

(Received October 13, 1999)

Publication Dates

History