Overview Dysmorphic, which literally means ‘abnormal form’, refers to an unusual appearance, usually of the face. Accurate syndrome diagnosis is important to give information about prognosis, associated problems, recurrence risk and support groups for families. Diagnoses are made by thorough clinical assessment followed by use of aids such as computerized syndrome databases.
Dysmorphic: Abnormal form, an unusal appearence, usually of the face
Syndrome: This is from the Greek ‘running together’ and refers to a cluster of physical and other features occurring in a consistent pattern, with an implied common specific cause that may be unknown.
Association: This is a group of physical features that tends to occur together but the link is not consistent enough to allow the term syndrome to be used. An example is the VATER association
Sequence: This refers to a group of abnormalities caused by a cascade of events beginning with
Definition Types of structural birth defects
Malformation arise during the initial formation of the embryo and fetus as a result of genetic and/ or environmental factors during organogenesis (2–8 weeks post-conception). Malformations may include failure of formation, incomplete formation or abnormal configuration. Examples include spina bifida, cleft palate and hypospadias.
Disruption result from a destructive process that alters structures after formation. Examples include early amnion rupture causing amputation defects of digits, and vasoconstriction defects caused by cocaine.
Deformations result from moulding of a part by mechanical forces, usually acting over a prolonged period. Examples include talipes, congenital hip dislocations and plagiocephaly associated with oligohydramnios.
- Teratogens, such as drugs, viruses, maternal diabetes, maternal hyperthermia
- Fetal movements – a neuromuscular disorder may cause reduced fetal movements, resulting in arthrogryposis
- Prenatal screening and diagnostic tests.
- weight, length, head circumference and Apgar scores at birth
- Growth and development, behaviour, sleep patterns.
- Behaviour and alertness
- Facial Features
- Palpebral fissures (Distance between eyes)
- Epicanthal folds
- Hyper or hypotelorism (distance between the two eyes)
- Iris (aniridia, coloboma)
- Fingers and Toes
- Syndactyly (Fused – simple, complex)
- Polydactyly (extra digits)
- Campylodactyly (bendy shape)
- Appropriate proportions of limbs
- Hand and Feet
- Single palmar crease
- Sandal toes
- Appropriate movement and positioning – equal
- Clavicular fracture
- Erbs or Klumkes
Pattern of Inheritance
- Autosomal recessive: both parents carriers, 1 in 4 chance of an affected child e.g. Cystic fibrosis
- Autosomal dominant: 1 in 2 chance of affected child e.g. NF
- X linked recessive: mutation in a gene on X chromosome. If mother is a carrier, 1 in 2 chance her sons will be affected and 1 in 2 chance her daughters will be carriers e.g. Duchenne muscular dystrophy
- Polygenic disorder: due to interaction of a number of genes e.g Cleft palate
|Remember Teratogen is an environmental agent that can cause abnormalities of form or function in an exposed embryo or fetus (examples: sodium valproate and alcohol). Estimated ~ 1% and 3% of birth defects may be related to teratogenic exposure.
- <2weeks after contraception – exposure of teratogen is likely to cause embronynic death rather than malformation (all or nothing effect)
- 2-8 weeks after contraception – During organogenesis exposure to teratogens may cause malformation
- >8 weeks after contraception – slowly forming organs such as brain and kidney can be effected by teratogen exposure resulting in cognitive impairment, or behavioral effects.
Common chromosomal disorders
- Down’s Syndrome (Trisomy 21)
- Edwards Syndrome (Trisomy 18)
- Patau syndrome (Trisomy 13)
- Turner Syndrome
- Klinfelters Syndrome (Additional X chromsome)
- Tripple X syndrome
- Fragile X syndrome
Other common disorders
- CHARGE Syndrome
- VACTERL association
- Noonan syndrome
- Marfan Syndrome
- Pierre Robin Sequence
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