Neonatal Progeroid Syndrome | Wiedemann Rautenstrauch Syndrome | Dr Irfan Mughal

Neonatal Progeroid Syndrome
Wiedemann Rautenstrauch Syndrome
Dr Irfan Mughal

Rare Genetic Disease.
Intrauterine growth restriction

Feeding difficulties

Distinctive craniofacial features

Hypotonia

Developmental delay

Mild to severe intellectual disability

Triangular face with a relatively large skull

Large anterior fontanelle,

Prominent veins especially on the scalp

Sparse scalp hair

Decreased eyebrows and eyelashes

Small mouth

Micrognathia

Old man facies

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