Two cases are reported of a boy and a girl with similar neurocutaneous syndromes clinically characterized by hyperpigmented skin patches and severe CNS involvement. The diagnosis of atypical cases of Incontinentia Pigmenti is suggested. The different syndromes with mental and motor retardation associated with skin abnormalities (Incontinentia Pigmenti, Ito's hypomelanosis, phakomatoses, etc.) are reviewed
Bloch-Sulzberger syndrome is a rare genetic disease that has both cutaneous and extra cutaneous mani...
Incontinentia pigmenti (IP) or Bloch-Sulzberger syndrome, is a rare X linked dominant disorder with ...
syndrome, is a neurocutaneous syndrome with neurological, ophthalmological and dental manifestations...
Two cases are reported of a boy and a girl with similar neurocutaneous syndromes clinically characte...
Incontinentia Pigmenti (IP) is a rare X-linked dominant disorder which is mostly lethal for males. I...
Incontinentia pigmenti is a genodermatosis with X-linked dominant inheritance, characterized by cuta...
IP is an uncommon X-linked dominant disorder (incidence: 1/40.000 newborn). It is caused by mutation...
Incontinentia Pigmenti (IP) is a rare X-linked dominant disorder with skin, eye, central nervous sys...
ncontinentia pigmenti (IP) is a rare X-linked dominant disease that is typically lethal to males and...
Incontinentia pigmenti is a rare X-linked neuroectodermal dysplasia estimated to occur in approximat...
Incontinentia Pigmenti (IP), (OMIM # 308300), is a rare X-linked dominant condition. It is a multisy...
Incontinentia pigmenti (IP) is an uncommon genodermatosis that usually occurs in female infants. It ...
ObjectiveIncontinentia Pigmenti (IP) (Bloch_Sulzberg syndrome) is a rare neurocutaneous syndrome cha...
A clinico-pathological and EM study of a Thai boy with hypomelanosis of Ito, one of the neurocuta-ne...
Incontinentia pigmenti (IP) is a rare genodermatoses with multisystem involvement. Monochorionic dia...
Bloch-Sulzberger syndrome is a rare genetic disease that has both cutaneous and extra cutaneous mani...
Incontinentia pigmenti (IP) or Bloch-Sulzberger syndrome, is a rare X linked dominant disorder with ...
syndrome, is a neurocutaneous syndrome with neurological, ophthalmological and dental manifestations...
Two cases are reported of a boy and a girl with similar neurocutaneous syndromes clinically characte...
Incontinentia Pigmenti (IP) is a rare X-linked dominant disorder which is mostly lethal for males. I...
Incontinentia pigmenti is a genodermatosis with X-linked dominant inheritance, characterized by cuta...
IP is an uncommon X-linked dominant disorder (incidence: 1/40.000 newborn). It is caused by mutation...
Incontinentia Pigmenti (IP) is a rare X-linked dominant disorder with skin, eye, central nervous sys...
ncontinentia pigmenti (IP) is a rare X-linked dominant disease that is typically lethal to males and...
Incontinentia pigmenti is a rare X-linked neuroectodermal dysplasia estimated to occur in approximat...
Incontinentia Pigmenti (IP), (OMIM # 308300), is a rare X-linked dominant condition. It is a multisy...
Incontinentia pigmenti (IP) is an uncommon genodermatosis that usually occurs in female infants. It ...
ObjectiveIncontinentia Pigmenti (IP) (Bloch_Sulzberg syndrome) is a rare neurocutaneous syndrome cha...
A clinico-pathological and EM study of a Thai boy with hypomelanosis of Ito, one of the neurocuta-ne...
Incontinentia pigmenti (IP) is a rare genodermatoses with multisystem involvement. Monochorionic dia...
Bloch-Sulzberger syndrome is a rare genetic disease that has both cutaneous and extra cutaneous mani...
Incontinentia pigmenti (IP) or Bloch-Sulzberger syndrome, is a rare X linked dominant disorder with ...
syndrome, is a neurocutaneous syndrome with neurological, ophthalmological and dental manifestations...