Otocephaly

Otocephaly with cyclopia and a proboscis

Grade 10 to 12 otocephaly in a dog and a pig; the face has been reduced to only the ears

The disorder is characterised by the absence of the mandible (agnathia), with the ears fused together just below the chin (synotia). In addition to agnathia and synotia, other symptoms that may manifest in otocephaly include:[2]

• Facial/musculoskeletal
  • Small (microglossia) or absent (aglossia) tongue
  • Small (microstomia) or absent (astomia) mouth
  • Cyclopia with proboscis
  • Median cleft lip and cleft palate
• Neurological
  • Holoprosencephaly
  • Agenesis of the corpus callosum
  • Anencephaly or other neural tube defects
• Organ systems
  • Situs inversus (full rotation of the internal organs)
  • Cardiac anomalies
  • Ambiguous genitalia
  • Absence of glands

Otocephaly is generally a result of a de novo mutation in the gene PRRX1 on the long arm of chromosome 1.[1] Autosomal trisomies, while prevalent in related conditions like cyclopia, are uncommon in otocephaly.

Otocephaly describes a spectrum of various manifestations, ranging in severity from severe micrognathia as a part of the Pierre Robin sequence to the cyclopia-holoprosencephaly complex, which is invariably associated with fetal death or death immediately after birth. Otocephaly is classified into four groups: (1) agnathia alone; (2) agnathia with holoprosencephaly; (3) agnathia with situs inversus and visceral anomalies; and (4) agnathia with holoprosencephaly, situs inversus, and visceral anomalies. Other extracranial malformations include neural tube defects, cephalocele, corpus callosum dysgenesis, renal ectopia, adrenal hypoplasia and rib, vertebral, or cardiac abnormalities.[5]

Because of the wide range of malformations, outcomes are variable. The most severe cases, often called cyclopia-holoprosencephaly complex, are almost invariably lethal, and patients show intrauterine growth retardation, prematurity, and impaired ventilation. Endotracheal intubation is difficult due to severe airway malformations, and only approximately 7 non-holoprosencephaly patients have survived beyond infancy.[6]

However, the less severe agnathia-otocephaly complex (AOC) has been successfully treated by extensive reconstructive surgery, including reconstruction of the mandible. Research indicates that a reasonable quality of life may even be achieved. However, the lack of musculature cannot be repaired with current therapies. This means swallowing is virtually impossible, so patients will depend on enteral nutrition. Researchers are optimistic that transplantation may eventually allow more complete reconstruction of structures affected by AOC.[7]

In all cases, an expert team, family information, premature birth planning, early gastrostomy and tracheostomy, and a long-term treatment plan are essential to ensure proper patient management.[8]

Otocephaly was first described in 1717 by Dutch scientist Theodor Kerckring. In 1933, evolutionary biologist Sewall Wright performed a study on otocephaly on guinea pigs and gave otocephaly its name.[3] The name comes from the Greek-derived New Latin prefix oto- ("ear") and the suffix -cephaly ("head").

In 2018, Indian neonatologist Kanwar Singh and his associates described a severe case of otocephaly with cyclopia, agnathia, complete astomia and synotia. They termed this severe presentation Kanwar syndrome.[2]

• NINDS Overview