Add to ORKGIncontinentia pigmenti (IP) or Bloch-Sulzberger syndrome, is a rare X linked dominant disorder with characteristic skin, hair, eye, dental and neurological abnormalities mostly affecting females. We reported two cases of newborn female children exhibiting characteristic cutaneous and neurological findings with one year follow-up.</p
BackgroundIncontinentia pigmenti (IP) is a rare X-linked dominant disorder that involves ectodermal ...
Incontinentia pigmenti (IP) is an uncommon genodermatosis that usually occurs in female infants. It ...
Incontinentia pigmenti is a rare X-linked genodermatosis that affects mainly female neonates. The fi...
ObjectiveIncontinentia Pigmenti (IP) (Bloch_Sulzberg syndrome) is a rare neurocutaneous syndrome cha...
Incontinentia pigmenti (IP) is a rare multisystem disease, X linked dominant disorder. As all X link...
Incontinentia Pigmenti (IP) is a rare X-linked dominant disorder which is mostly lethal for males. I...
Incontinentia pigmenti (IP) is a rare multisystem disease, X linked dominant disorder. As all X link...
Bloch-Sulzberger syndrome is a rare genetic disease that has both cutaneous and extra cutaneous mani...
Incontinentia Pigmenti is an uncommon X-linked genodermatosis, caused by mutations in the NEMO gene....
Incontinentia pigment! (Bloch-Sulzberger syndrome) is a rare neuroectodermal dysptasia. It is an X-l...
Incontinentia Pigmenti (IP), (OMIM # 308300), is a rare X-linked dominant condition. It is a multisy...
Linear skin lesions were noticed at birth in a baby girl, first born to a young mother. The lesions ...
Abstract: Incontinentia pigmenti is a rare X-linked genodermatosis that affects mainly female neonat...
Incontinentia pigmenti is a genodermatosis with X-linked dominant inheritance, characterized by cuta...
ncontinentia pigmenti (IP) is a rare X-linked dominant disease that is typically lethal to males and...
BackgroundIncontinentia pigmenti (IP) is a rare X-linked dominant disorder that involves ectodermal ...
Incontinentia pigmenti (IP) is an uncommon genodermatosis that usually occurs in female infants. It ...
Incontinentia pigmenti is a rare X-linked genodermatosis that affects mainly female neonates. The fi...
ObjectiveIncontinentia Pigmenti (IP) (Bloch_Sulzberg syndrome) is a rare neurocutaneous syndrome cha...
Incontinentia pigmenti (IP) is a rare multisystem disease, X linked dominant disorder. As all X link...
Incontinentia Pigmenti (IP) is a rare X-linked dominant disorder which is mostly lethal for males. I...
Incontinentia pigmenti (IP) is a rare multisystem disease, X linked dominant disorder. As all X link...
Bloch-Sulzberger syndrome is a rare genetic disease that has both cutaneous and extra cutaneous mani...
Incontinentia Pigmenti is an uncommon X-linked genodermatosis, caused by mutations in the NEMO gene....
Incontinentia pigment! (Bloch-Sulzberger syndrome) is a rare neuroectodermal dysptasia. It is an X-l...
Incontinentia Pigmenti (IP), (OMIM # 308300), is a rare X-linked dominant condition. It is a multisy...
Linear skin lesions were noticed at birth in a baby girl, first born to a young mother. The lesions ...
Abstract: Incontinentia pigmenti is a rare X-linked genodermatosis that affects mainly female neonat...
Incontinentia pigmenti is a genodermatosis with X-linked dominant inheritance, characterized by cuta...
ncontinentia pigmenti (IP) is a rare X-linked dominant disease that is typically lethal to males and...
BackgroundIncontinentia pigmenti (IP) is a rare X-linked dominant disorder that involves ectodermal ...
Incontinentia pigmenti (IP) is an uncommon genodermatosis that usually occurs in female infants. It ...
Incontinentia pigmenti is a rare X-linked genodermatosis that affects mainly female neonates. The fi...