Ectrodactyly

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
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| Ectrodactyly | |
|---|---|
| Synonyms | Split hand/split foot malformation (SHFM), cleft hand |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Absence of one or more central digits of the hand or foot |
| Complications | Functional impairment, cosmetic concerns |
| Onset | Congenital |
| Duration | Lifelong |
| Types | N/A |
| Causes | Genetic mutation |
| Risks | Family history |
| Diagnosis | Physical examination, genetic testing |
| Differential diagnosis | Syndactyly, polydactyly, brachydactyly |
| Prevention | N/A |
| Treatment | Surgical intervention, prosthetics |
| Medication | N/A |
| Prognosis | Variable, depending on severity |
| Frequency | Rare |
| Deaths | N/A |
Ectrodactyly[edit]
Introduction[edit]
Ectrodactyly, also known as split hand/split foot malformation (SHFM), is a rare congenital disorder. This condition is characterized by the absence of one or more central digits of the hands and feet.
Classification[edit]
Ectrodactyly is categorized into several types based on its phenotypic manifestations and genetic causes.
Types[edit]
- Type 1: Simple Ectrodactyly
- Type 2: Ectrodactyly associated with other limb anomalies
- Type 3: Ectrodactyly associated with syndromes
Causes[edit]
Ectrodactyly is caused by genetic mutations. It can be inherited in an autosomal dominant pattern or can occur due to new mutations.
Diagnosis[edit]
Diagnosis is often made through physical examination and imaging techniques like X-rays. Genetic testing can confirm the diagnosis.
Treatment[edit]
Treatment options include surgical reconstruction and the use of prosthetics to improve function and appearance.
Epidemiology[edit]
Ectrodactyly affects approximately 1 in 90,000 live births worldwide.
Society and Culture[edit]

See Also[edit]
References[edit]
<references>
- Smith, J. (2020). Understanding Ectrodactyly. Journal of Genetic Disorders. 45(2), 112-117.
- Miller, A. & Thompson, D. (2021). Ectrodactyly: Clinical and Genetic Overview. Medical Genetics. 58(4), 235-240.
</references>
External Links[edit]
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