Pitt–Hopkins syndrome

Pitt–Hopkins syndrome (PTHS) is a rare genetic disorder characterized by developmental delay, epilepsy, distinctive facial features, and possible intermittent hyperventilation followed by apnea.[1] As more is learned about Pitt–Hopkins, the developmental spectrum of the disorder is widening, and can also include difficulties with anxiety, autism,[2] ADHD, and sensory disorders. It is associated with an abnormality within chromosome 18; specifically, it is caused by an insufficient expression of the TCF4 gene.[3]

Pitt–Hopkins syndrome
Boy with Pitt–Hopkins syndrome showing the characteristic facial features
SpecialtyPsychiatry, Medical genetics

PTHS has traditionally been associated with severe cognitive impairment, however true intelligence is difficult to measure given motor and speech difficulties. Thanks to augmentative communication and more progressive therapies, many individuals can achieve much more than initially thought. It has become clearer that there is a wider range of cognitive abilities in Pitt–Hopkins than reported in much of the scientific literature. Researchers have developed cell and rodent models to test therapies for Pitt–Hopkins.[4]

Signs and symptoms

PTHS can be seen as early as childhood.[5]

The earliest signs in infants is the lower face and the high nasal root.[6]

The facial features are characteristic and include:

  • Deep set eyes
  • Strabismus
  • Myopia
  • Marked nasal root
  • Broad and/or beaked nasal bridge
  • Prominent Cupid's bow or tented upper lip (upper lip with the appearance of a tent)
  • Everted lower lip
  • Large mouth
  • Widely spaced teeth
  • Wide and shallow palate
  • Ears with a thick and overfolded helix (the outermost fold of the ear)

Adults who have PTHS may have trouble with their speech.[5] Craniofacial features, which are important when diagnosing PTHS, become more visible as the person gets older.[6]

PTHS is characterized by developmental delay, possible breathing problems of episodic hyperventilation and/or breath-holding while awake, recurrent seizures/epilepsy, gastrointestinal issues, and distinctive facial features. Stereotypic movements, particularly of the arms, wrists and fingers are almost universal. Hypotonia is common (75%), as is an unsteady gait. Other features include a single (simian) palmar crease, long, slender fingers, flat feet and cryptorchidism (in males). The presence of "fetal finger pads" is common. Hyperventilation may occur and is sometimes followed by apnea and cyanosis. Constipation is common. Microcephaly and seizures may occur. Hypopigmented skin macules have occasionally been reported. Individuals with Pitt–Hopkins syndrome typically have a happy, excitable demeanor with frequent smiling and laughter.

Genetics

The condition was first described in 1978 by D. Pitt and I. Hopkins (The Children's Cottages Training Centre, Kew and Royal Children's Hospital, Melbourne, Australia) in two unrelated patients.[7]

The genetic cause of this disorder was described in 2007.[8] This disorder is due to a haploinsufficiency of the transcription factor 4 (TCF4) gene which is located on the long arm of chromosome 18 (18q21.2) The mutational spectrum appears to be 40% point mutations, 30% small deletions/insertions and 30% deletions. All appear to be de novo mutations. The risk in siblings is low, but higher than the general population due to parental germline mosaicism.[6]

A Pitt–Hopkins-like phenotype has been assigned to autosomal recessive mutations of the contactin associated protein like 2 (CNTNAP2) gene on the long arm of chromosome 7 (7q33-q36) and the neurexin 1 alpha (NRXN1) gene on the short arm of chromosome 2 (2p16.3).[9]

Malformations in the CNS can be seen in about 60 to 70% of patients on MRI scans.[10]

Pitt–Hopkins patients with a TCF4 deletion can lack the syndrome's characteristic facial features.[6]

Diagnosis

There is not a certain diagnostic criteria, but there are a few symptoms that support a diagnosis of PTHS. Some examples are: facial dysmophism, early onset global developmental delay, moderate to severe intellectual disability,breathing abnormalities, and a lack of other major congenital abnormalities.[5]

Half of the individuals with PTHS are reported to have seizures, starting from childhood to the late teens.[6]

Around 50% of those affected show abnormalities on brain imaging. These include a hypoplastic corpus callosum with a missing rostrum and posterior part of the splenium, with bulbous caudate nuclei bulging towards the frontal horns.

Electroencephalograms show an excess of slow components.

According to the clinical diagnosis. PTHS is in the same group as Pervasive Developmental Disorders.[11]

Evaluations[6]

  • Developmental assessment
  • Assessment for communication devices
  • Child behavior specialist
  • Pulmonary consultation
  • Child neurology consultation
  • Ophthalmology evaluation
  • Gastroenterology
  • Musculoskeletal evaluation
  • Clinical geneticist

Differential diagnosis

Differential diagnosis includes Angelman syndrome, Rett syndrome and Mowat–Wilson syndrome.[10]

Angelman syndrome most closely resembles PTHS. Both have absent speech and a "happy" disposition. One thing they do not have in common is facial abnormalities. Of the differentials, Rett syndrome is the least close to PTHS. This syndrome is seen as a progressive encephalopathy. Mowat–Wilson syndrome is seen in early infancy and is characterized by distinctive facial abnormalities.[10]

Treatment

Currently there is no specific treatment for this condition. It is based on symptomatology. Since there is a lack of treatment, people with PTHS use behavioral and training approaches.[11]

Recommendations for developmental delay and intellectual disability in the U.S. (may differ depending on country):[6]

  • Early intervention program from newborn to age 3 will allow access to different therapies (occupational, physical, speech, and feeding).
  • Developmental preschool through public school systems from ages 3 to 5. The child will need an evaluation before getting into the program, to see what kind of therapy is needed.
  • From the ages 5–21 the child's school may create an IEP (based on the child's functions and needs). Children are encouraged to stay in school until at least the age of 21.

History
Peter the Wild Boy, showing some of the physical traits of Pitt–Hopkins syndrome, including coarse, curly hair, drooping eyelids and large, thick-lipped mouth

Professor Philip Beales, of the Institute of Child Health, has speculated that Peter the Wild Boy suffered from Pitt–Hopkins syndrome.[12] The boy was brought to Britain in 1725 as a feral child.

See also

References
  1. Zweier C, Peippo MM, Hoyer J, et al. (May 2007). "Haploinsufficiency of TCF4 causes syndromal mental retardation with intermittent hyperventilation (Pitt–Hopkins syndrome)". American Journal of Human Genetics. 80 (5): 994–1001. doi:10.1086/515583. PMC 1852727. PMID 17436255.
  2. "Pitt-Hopkins syndrome may point the way to autism treatments". DANIEL R. WEINBERGER.
  3. "PITT-HOPKINS SYNDROME; PTHS". National Center for Biotechnology Information. Retrieved 2009-12-08.
  4. "A drug for autism? Potential treatment for Pitt-Hopkins syndrome offers clues; PTHS". The Conversation (website). Retrieved 2019-07-10.
  5. Dean L (2012). "Pitt-Hopkins Syndrome". In Pratt VM, McLeod HL, Rubinstein WS, et al. (eds.). Medical Genetics Summaries. National Center for Biotechnology Information (NCBI). PMID 28520343. Bookshelf ID: NBK66129.
  6. Sweetser, David A.; Elsharkawi, Ibrahim; Yonker, Lael; Steeves, Marcie; Parkin, Kimberly; Thibert, Ronald (1993), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "Pitt-Hopkins Syndrome", GeneReviews®, University of Washington, Seattle, PMID 22934316, retrieved 2019-02-03
  7. Pitt D, Hopkins I (1978) A syndrome of mental retardation, wide mouth and intermittent overbreathing. Aust Paed J 14(3):182-184
  8. Amiel J, Rio M, de Pontual L, Redon R, Malan V, Boddaert N, Plouin P, Carter NP, Lyonnet S, Munnich A, Colleaux L (2007) Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunction. Am. J. Hum. Genet. 80: 988-993
  9. M, Peippo; J, Ignatius (April 2012). "Pitt-Hopkins Syndrome". Molecular Syndromology. 2 (3–5): 171–180. doi:10.1159/000335287. PMC 3366706. PMID 22670138.
  10. Zollino, Marcella; Marangi, Giuseppe (September 2015). "Pitt–Hopkins Syndrome and Differential Diagnosis: A Molecular and Clinical Challenge". Journal of Pediatric Genetics. 04 (3): 168–176. doi:10.1055/s-0035-1564570. ISSN 2146-4596. PMC 4918722. PMID 27617128.
  11. Sweatt, J. David (May 2013). "Pitt–Hopkins Syndrome: intellectual disability due to loss of TCF4-regulated gene transcription". Experimental & Molecular Medicine. 45 (5): e21. doi:10.1038/emm.2013.32. ISSN 2092-6413. PMC 3674405. PMID 23640545.
  12. Megan Lane (8 August 2011). "Who was Peter the Wild Boy?". BBC News Magazine. BBC. Retrieved 2011-08-09.
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External resources
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