Chromosome 19q13.11 deletion syndrome

MONDO:0013090

The 19q13.11 microdeletion is characterized by several major features including pre and postnatal growth retardation, slender habitus, severe postnatal feeding difficulties, microcephaly, intellectual deficit with speech disturbance, hypospadias and ectodermal dysplasia presented by scalp aplasia, thin and sparse hair, eyebrows and eyelashes, thin and dry skin and dysplasic nails.

Also known as: 19q13.11 microdeletion syndrome, Del(19)(q13.11), monosomy 19q13.11, chromosome 19Q13.11 deletion syndrome, distal, chromosome 19q13.11 deletion syndrome, distal

0 clinical trials for this condition and its sub-types, 0 tagged with Chromosome 19q13.11 deletion syndrome itself.

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↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59) ↑ Partial deletion of the long arm of chromosome 19 (0)

Sub-types of Chromosome 19q13.11 deletion syndrome

Chromosome 19q13.11 deletion syndrome, distal 0 trials
Chromosome 19q13.11 deletion syndrome, proximal 0 trials

Including sub-types (0) Tagged with Chromosome 19q13.11 deletion syndrome (0)

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