Sasi Bhushan Gottimukkala, Madhu Jagalasar, Giridhar Sethuraman, Srinivasan Kitchanan Department of Neonatology, Chettinad Hospital & Research Institute, Chennai, Tamil Nadu, India Abstract: Incontinentia pigmenti is a rare X-linked dominant multi-system disorder that is clinically suspected, based on the characteristic evolution of skin lesions through four stages. We describe a term neonate who presented at birth with pleomorphic skin rashes, including linear hyperpigmented hyperkeratotic lesions and erythematous vesicles, and then developed seizures. She was later histologically and genetically confirmed as a case of incontinentia pigmenti. The simultaneous presence of three stages of skin lesions in the neonatal period is an atypic...
Incontinentia pigmenti is a rare, X-linked dominant multisys-tem genodermatosis affecting ectodermal...
CASE PRESENTATION: A substance abusing G2P1 mother spontaneously delivered at term an appropriate fo...
Incontinentia pigmenti (IP) is an X-linked dominant neurocutaneous syndrome with ophthalmologic, neu...
Incontinentia pigmenti (IP) is a rare genetic multisystem disorder that may affect many organs inclu...
Incontinentia pigmenti is a rare X-linked neuroectodermal dysplasia estimated to occur in approximat...
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), (OMIM # 308300), is a rare X-linked dominant condition. It is a multisy...
syndrome, is a neurocutaneous syndrome with neurological, ophthalmological and dental manifestations...
Summary: Incontinentia pigmenti is a rare neurocutaneous disorder that may present with neurologic s...
Incontinentia pigmenti (IP) is a rare multisystem disease, X linked dominant disorder. As all X link...
Linear vesicles or papules in a newborn can be a presenting sign of incontinentia pigmenti (IP). In ...
ObjectiveIncontinentia Pigmenti (IP) (Bloch_Sulzberg syndrome) is a rare neurocutaneous syndrome cha...
Incontinentia Pigmenti (IP) is a rare X-linked dominant disorder with skin, eye, central nervous sys...
Abstract: Incontinentia pigmenti is a rare X-linked genodermatosis that affects mainly female neonat...
Incontinentia pigmenti is a rare, X-linked dominant multisys-tem genodermatosis affecting ectodermal...
CASE PRESENTATION: A substance abusing G2P1 mother spontaneously delivered at term an appropriate fo...
Incontinentia pigmenti (IP) is an X-linked dominant neurocutaneous syndrome with ophthalmologic, neu...
Incontinentia pigmenti (IP) is a rare genetic multisystem disorder that may affect many organs inclu...
Incontinentia pigmenti is a rare X-linked neuroectodermal dysplasia estimated to occur in approximat...
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), (OMIM # 308300), is a rare X-linked dominant condition. It is a multisy...
syndrome, is a neurocutaneous syndrome with neurological, ophthalmological and dental manifestations...
Summary: Incontinentia pigmenti is a rare neurocutaneous disorder that may present with neurologic s...
Incontinentia pigmenti (IP) is a rare multisystem disease, X linked dominant disorder. As all X link...
Linear vesicles or papules in a newborn can be a presenting sign of incontinentia pigmenti (IP). In ...
ObjectiveIncontinentia Pigmenti (IP) (Bloch_Sulzberg syndrome) is a rare neurocutaneous syndrome cha...
Incontinentia Pigmenti (IP) is a rare X-linked dominant disorder with skin, eye, central nervous sys...
Abstract: Incontinentia pigmenti is a rare X-linked genodermatosis that affects mainly female neonat...
Incontinentia pigmenti is a rare, X-linked dominant multisys-tem genodermatosis affecting ectodermal...
CASE PRESENTATION: A substance abusing G2P1 mother spontaneously delivered at term an appropriate fo...
Incontinentia pigmenti (IP) is an X-linked dominant neurocutaneous syndrome with ophthalmologic, neu...