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Plagiocephaly, also known as flat head syndrome, is a condition characterized by an asymmetrical distortion (flattening of one side) of the
skull The skull, or cranium, is typically a bony enclosure around the brain of a vertebrate. In some fish, and amphibians, the skull is of cartilage. The skull is at the head end of the vertebrate. In the human, the skull comprises two prominent ...
. A mild and widespread form is characterized by a flat spot on the back or one side of the head caused by remaining in a
supine position The supine position () means lying horizontally, with the face and torso facing up, as opposed to the prone position, which is face down. When used in surgical procedures, it grants access to the peritoneal, thoracic, and pericardium, pericardial ...
for prolonged periods. Plagiocephaly is a diagonal asymmetry across the head shape. Often it is a flattening which is to one side at the back of the head, and there is often some facial asymmetry. Depending on whether synostosis is involved, plagiocephaly divides into two groups: synostotic, with one or more fused cranial sutures, and non-synostotic (deformational). Surgical treatment of these groups includes the deference method; however, the treatment of deformational plagiocephaly is controversial.
Brachycephaly Brachycephaly (derived from the Ancient Greek '' βραχύς'', 'short' and '' κεφαλή'', 'head') is the shape of a skull shorter than average in its species. It is perceived as a cosmetically desirable trait in some domesticated dog and ...
describes a very wide head shape with a flattening across the whole back of the head.


Causes

Slight plagiocephaly is routinely diagnosed at birth and may be the result of a restrictive intrauterine environment giving a "diamond" shaped head when seen from above. If there is premature union of skull bones, this is more properly called
craniosynostosis Craniosynostosis is a condition in which one or more of the fibrous sutures in a young infant's skull prematurely fuses by turning into bone (ossification), thereby changing the growth pattern of the skull. Because the skull cannot expand perpe ...
. The incidence of plagiocephaly has increased dramatically since the advent of anti- sudden infant death syndrome recommendations for parents to keep their babies on their backs. Data also suggest that the rates of plagiocephaly are higher for twins and multiple births, premature babies, babies who were positioned in the breech position or back-to-back, as well as for babies born after a prolonged labour.


Conditions and syndromes

Plagiocephaly is seen in multiple conditions: *
Arthrogryposis Arthrogryposis (AMC) describes congenital joint contracture in two or more areas of the body. It derives its name from Greek, literally meaning 'curving of joints' (', 'joint'; ', late Latin form of late Greek ', 'hooking'). Children born with one ...
,
cleft palate A cleft lip contains an opening in the upper lip that may extend into the nose. The opening may be on one side, both sides, or in the middle. A cleft palate occurs when the palate (the roof of the mouth) contains an opening into the nose. The ...
, craniosynostosis, and impaired intellectual development *
Autism spectrum disorder Autism, also known as autism spectrum disorder (ASD), is a neurodevelopmental disorder characterized by differences or difficulties in social communication and interaction, a preference for predictability and routine, sensory processing di ...
, susceptibility to, X-linked 2 * Blepharophimosis-impaired intellectual development syndrome * Cardiac anomalies - developmental delay - facial dysmorphism syndrome * CHIME syndrome * Coffin-Siris syndrome 1 and 6 * Congenital nonprogressive myopathy with Moebius and Robin sequences * Cornelia de Lange syndrome 3 *
Cranioectodermal dysplasia Sensenbrenner syndrome (OMIM #218330) is a rare (less than 20 cases reported by 2010) multisystem disease first described by Judith A. Sensenbrenner in 1975. It is inherited in an autosomal recessive fashion, and a number of genes appear to be resp ...
2 * Craniosynostosis (nonsyndromic) 6 * Developmental and epileptic
encephalopathy Encephalopathy (; ) means any disorder or disease of the brain, especially chronic degenerative conditions. In modern usage, encephalopathy does not refer to a single disease, but rather to a syndrome of overall brain dysfunction; this syndrome ...
, 1, 65, 77, and 84 * Developmental delay with variable
intellectual impairment Developmental disability is a diverse group of chronic conditions, comprising mental or physical impairments that arise before adulthood. Developmental disabilities cause individuals living with them many difficulties in certain areas of life, espe ...
and behavioral abnormalities * Dihydropyrimidinase deficiency * Early-onset progressive diffuse
brain atrophy Cerebral atrophy is a common feature of many of the diseases that affect the brain. Atrophy of any tissue means a decrement in the size of the cell, which can be due to progressive loss of cytoplasmic proteins. In brain tissue, atrophy describes ...
- microcephaly- muscle weakness- optic atrophy syndrome * Faciocardiorenal syndrome *
FG syndrome FG syndrome (FGS) is a rare genetic syndrome caused by one or more recessive genes located on the X chromosome and causing physical anomalies and developmental delays. FG syndrome was named after the first letters of the surnames of the first pat ...
* Galloway-Mowat syndrome 4 * Gaze palsy, familial horizontal, with progressive
scoliosis Scoliosis (: scolioses) is a condition in which a person's Vertebral column, spine has an irregular curve in the coronal plane. The curve is usually S- or C-shaped over three dimensions. In some, the degree of curve is stable, while in others ...
1 * Hyperphosphatasia with intellectual disability syndrome 1 and 2 *
Hypotonia Hypotonia is a state of low muscle tone (the amount of tension or resistance to stretch in a muscle), often involving reduced muscle strength. Hypotonia is not a specific medical disorder, but it is a potential manifestation of many different dis ...
, infantile, with psychomotor retardation and characteristic facies 2 * Intellectual developmental disorder, autosomal dominant 64 and 66 * Intellectual disability, autosomal dominant 13, 40, 48, and 58 * Joubert syndrome 1 * Kleefstra syndrome 2 * Langer-Giedion syndrome * Microphthalmia with brain and digit anomalies * Mitochondrial DNA depletion syndrome 13 * Muenke syndrome * Noonan syndrome 13 *
Osteogenesis imperfecta Osteogenesis imperfecta (; OI), colloquially known as brittle bone disease, is a group of genetic disorders that all result in bones that bone fracture, break easily. The range of symptoms—on the skeleton as well as on the body's other Or ...
, type 20 * Ritscher-Schinzel syndrome 4 * Saethre-Chotzen syndrome *
Spastic paraplegia Hereditary spastic paraplegia (HSP) is a group of inherited diseases whose main feature is a progressive Gait abnormality, gait disorder. The disease presents with progressive stiffness (spasticity) and contraction in the lower limbs. HSP is als ...
, intellectual disability, nystagmus, and
obesity Obesity is a medical condition, considered by multiple organizations to be a disease, in which excess Adipose tissue, body fat has accumulated to such an extent that it can potentially have negative effects on health. People are classifi ...
* Syndromic X-linked intellectual disability Najm type


Diagnosis

A developmental and physical assessment performed by a physician or a pediatric specialist is recommended. Often, imaging is obtained if the diagnosis is questionable to see if the baby's sutures are present or not. If the sutures are not present,
craniosynostosis Craniosynostosis is a condition in which one or more of the fibrous sutures in a young infant's skull prematurely fuses by turning into bone (ossification), thereby changing the growth pattern of the skull. Because the skull cannot expand perpe ...
may be ruled into question. It is also common for an infant with positional plagiocephaly to have misaligned ears (the ear on the affected side may be pulled forward and down and be larger or protrude more than the unaffected ear). Plagiocephaly Greig.jpg, Left anterior plagiocephaly Plagiocephaly or Asymmetrical Skull.jpg, Right anterior plagiocephaly Plagiocéphalie.JPG, Left posterior plagiocephaly (positional case) Плагиоцефалия.jpg, Right posterior plagiocephaly


Prevention

Prevention methods include carrying the infant and giving the infant time to play on their stomach ( tummy time), which may prevent the baby from progressing into moderate or severe plagiocephaly. Letting babies crawl may also prove to be crucial in preventing plagiocephaly as it strengthens babies' spine and neck muscles. Crawling also boosts gross and fine motor skills (large and refined movements), balance, hand-eye coordination, and overall strength. In addition, specialized mattresses are available to prevent plagiocephaly. The design of these mattresses is characterized by an ergonomic design that reduces pressure on the baby's head. These mattresses must be certified to guarantee their effectiveness.


Treatment

The condition may improve to some extent as the baby grows, but in some cases, home treatment or physical therapy treatment can improve the shape of a baby's head. Early interventions (based on the severity) are important to reduce the severity of the degree of plagiocephaly. Diagnosis is most commonly determined through clinical examination. To assess the severity of the condition and determine the best course of treatment, practitioners often use the Plagiocephaly Severity Scale. This is a scale that can help practitioners evaluate the condition in a standardized way. The course of treatment is typically based on the age of the child when the diagnosis is made in conjunction with the severity of the diagnosis. If a diagnosis of mild to moderate plagiocephaly occurs before four months of age, repositioning therapy may be helpful. If the diagnosis is determined to be severe, practitioners will likely prescribe a cranial molding orthosis (helmet), which has the best results when prescribed between five and six months of age.


Repositioning

Initially, treatment usually takes the form of reducing the pressure on the affected area by repositioning the baby onto the abdomen for extended periods throughout the day. This may include repositioning the child's head throughout the day so that the rounded side of the head is placed against the mattress, repositioning cribs and other areas that infants spend time in so that they will have to look in a different direction to see their parents or others in the room, repositioning mobiles and other toys for similar reasons, and avoiding extended time sleeping in car seats (when not in a vehicle), bouncy seats, or other
supine In grammar, a supine is a form of verbal noun used in some languages. The term is most often used for Latin, where it is one of the four principal parts of a verb. The word refers to a position of lying on one's back (as opposed to ' prone', l ...
seating which is thought to exacerbate the problem. If the child appears to have discomfort or cries when they are repositioned, a neck problem should be ruled out.


Helmets

High-quality evidence is lacking for cranial remolding orthosis (baby helmet) for the positional condition and use for this purpose is controversial. If conservative treatment is unsuccessful, helmets may help to correct abnormal head shapes. These helmets are used to treat deformational plagiocephaly,
brachycephaly Brachycephaly (derived from the Ancient Greek '' βραχύς'', 'short' and '' κεφαλή'', 'head') is the shape of a skull shorter than average in its species. It is perceived as a cosmetically desirable trait in some domesticated dog and ...
, scaphocephaly, and other head shape deformities in infants 3–18 months of age by gently allowing the head shape to grow back into a normal shape. This type of treatment has been used for severe deformations.


Prognosis

Preliminary research indicates that some babies with plagiocephaly may comprise a high-risk group for developmental difficulties. Plagiocephaly is associated with motor and language developmental delays. While developmental delay is more commonplace among babies with plagiocephaly, it cannot be inferred that plagiocephaly is the cause of the delay.


Etymology

Ancient Greek Ancient Greek (, ; ) includes the forms of the Greek language used in ancient Greece and the classical antiquity, ancient world from around 1500 BC to 300 BC. It is often roughly divided into the following periods: Mycenaean Greek (), Greek ...
πλάγιος (''plagios'') 'oblique, slanting', from PIE ''plag-'' 'flat, spread', from *''plak-'', and Modern Latin ''cephal-'' 'head, skull, brain' (from Greek κεφαλή), together means 'flat head'.


See also

* Artificial cranial deformation * Yakovlevian torque


References


External links

{{Congenital malformations and deformations of musculoskeletal system Congenital disorders of musculoskeletal system