Holoprosencephaly

Holoprosencephaly (HPE) is a rare congenital brain malformation, resulting from incomplete separation of the two hemispheres.

Classically three sub types have been recognised, however additional entities are now included in the spectrum of the disease. The three main sub types, in order of decreasing severity are :

1. alobar holoprosencephaly
2. semilobar holoprosencephaly
3. lobar holoprosencephaly

Other entities

• syntelecephaly (or middle interhemispheric variant (MIH))
• septo optic dysplasia
• other
  • central incisor syndrome
  • non-specific midline dysplasia
  • frontonasal dysplasia
  • agnathia-otocephaly

This article is a general discussion of holoprosencephaly, with a more detailed discussion of individual radiographic features relegated to individual articles.  

Epidemiology

Although rare in absolute terms, holoprosencephaly is the most common forebrain abnormality and is seen in 1 per 10,000 - 16,000 live births ³. The early embryonic occurrence may be even higher but may not be detected due to most fetuses aborting in early gestation.

Clinical presentation

It is usually obvious at birth even if antenatal diagnosis has not been made, due to associated midline facial anomalies including ³:

• proboscis
• cyclopia
• cleft lip and / or palate
• ocular hypotelorism
• solitary median maxillary central incisor

Additionally these children also have systemic problems, with poor feeding, hypothalamic / pituitary dysfunction and developmental delay ³.

Pathology

The fundamental problem is a failure of the developing brain to divide into left and right halves (which normally occurring at the end of the 5^th week of gestation). This results in variable loss of midline structures of the brain and face as well as fusion of lateral ventricles and the 3^rd ventricle.. 

Environmental factors such as maternal diabetes mellitus, alcohol use, and retinoic acid have been implicated in the pathogenesis, as has mutation of a number of genes including Sonic hedgehog and ZIC2, on chromosome 13q32, (the latter also implicated in syntelencephaly) ^5-6. 

Associations

Recognised associations include

• aneuploidic / chromosomal
  • trisomy 13 :  most common genetic abnormality associated with holoprosencephaly ⁴
  • trisomy 18 
  • chromosome 7q deletion ⁸
  • chromosome 2q deletion ⁸
• non aneuploidic
  • congenital renal anomalies
  • congenital cardiac anomalies
  • diabetic embryopathy
  • facial anomalies
  • Shprintzen syndrome

Radiographic features

As with most cerebral structural congenital abnormalities, holoprosencephaly is visible on all modalities, but in general is identified on antenatal ultrasound (if performed), and best characterised by MRI. On antenatal ultrasound there may be also evidence of polyhydramnios an secondary feature due to impaired fetal swallowing.

Below are brief descriptions of the three main types. Note should be made that these are along a spectrum and as such some patients can be on the border between two types. 

Alobar holoprosencephaly

In alobar holoprosencephaly, the thalami are fused and there is a single large posteriorly located ventricle. Most commonly associated with facial abnormalities such as cyclopia, ethmocephaly, cebocephaly, and median cleft lip.

For more details see the article on alobar holoprosencephaly 

Semi-lobar holoprosencephaly

Here the basic structure of the cerebral lobes are present, but are fused most commonly anteriorly and at the thalami. The olfactory tracts and bulbs are usually not present, and there is agenesis or hypoplasia of the corpus callosum.

For more details see the article on semi-lobar holoprosencephaly 

Lobar holoprosencephaly

This is the least affected sub type. Patients demonstrate more subtle areas of midline abnormalities such as fusion of the cingulate gyrus and thalami. The olfactory tracts are absent or hypoplastic. There may be hypoplasia or absence of the corpus callosum.

For more details see the article on lobar holoprosencephaly 

Prognosis

The prognosis is dependant on the type of holoprosencephaly with almost all alobar and semilobar forms incomplatible with a extra uterine life. There may be recurrence risk for ~  6 % with non chromosomal sporadic holoproseccephaly.

Differential diagnosis

The differential diagnosis largely depends on the type, and as such please refer to the individual articles above.