hrp0098p3-43 | Bone, Growth Plate and Mineral Metabolism | ESPE2024

About a case of Trichorhinophalangien Syndrome

Rouabah Nadira , Rouabah Hamza , Bouamama Fatima , Messasset Mouna , Bioud Belkacem

Introduction: Trichorhinophalangeal syndrome (TRPS) is a rare autosomal dominant genetic disorder defined by craniofacial, ectodermal and skeletal involvement.Materials and Methods: She is a girl aged 07 years, the second in a sibling of 4 from a non-consanguineous couple. Physiological antecedents, full term birth with a low birth weight of 02 Kg, artificial breastfeeding from birth, good pshycomotor development with a ...

hrp0098p3-187 | Multisystem Endocrine Disorders | ESPE2024

Hypophosphaemic rickets, central precocious puberty and epidermic neavus syndrome.

Rouabah Nadira , Rouabah Hamza , Fellahi Meriem , Hassanine Assia , Messasset Mouna , Bioud Belkacem

Introduction: The association of multisystem pathologic conditions and epidermal nevi, known as the epidermal nevus syndrome, includes disorders of bone, central nervous system, eye, kidney, vasculature, body symmetry, and skin. Rarely hypophosphatemic trickets has been observed in association with this syndrome. Precocious puberty is another rare finding associated with epidermal nevus syndrome, having been observed in 1 patient.<strong...