Central precocious puberty

Central precocious puberty (CPP), also referred to as gonadotropin dependent precocious puberty, is an endocrine-related developmental disease characterized by the onset of pubertal changes, with development of secondary sexual characteristics and accelerated growth and bone maturation, before the normal age of puberty (8 years in girls and 9 years in boys).

Hypothalamic hamartoma

The presence of a hamartoma of the hypothalamus.


合計: 19

                      


(表示件数)
PMID (PMCID)
30470962
OTHER
Brief Behavioral Intervention for Disruptive Behavior in a Child with a Hypothalamic Hamartoma: A Case Report.
Fein RH, Banks GG, Gragert MN, Axelrad ME.
J Clin Psychol Med Settings. 2018;:.
Most children with hypothalamic hamartoma (HH) manifest symptoms of epilepsy and associated cognitive deficits and behavioral difficulties as well as central precocious puberty (CPP).
26028458
MALE Child
ADHD-like behavior in a patient with hypothalamic hamartoma.
Katayama K, Yamashita Y, Yatsuga S, Koga Y, Matsuishi T.
Brain Dev. 2016;38(1):145-8.
We report a male patient with hypothalamic hamartoma (HH) who manifested central precocious puberty (CPP) at 4 years of age.
25241615
(4293650)
MALE Child
A case of central precocious puberty due to concomitant hypothalamic hamartoma and juvenile pilocytic astrocytoma.
Catl G, Abac A, Ank A, Guleryuz H, Ozer E, Ocal I, Yuceer N, Mutafoglu K.
J Clin Res Pediatr Endocrinol. 2014;6(3):183-6.
A case of central precocious puberty due to concomitant hypothalamic hamartoma and juvenile pilocytic astrocytoma.
23934638
FEMALE
Hypothalamic hamartoma associated with central precocious puberty and growth hormone deficiency.
Rousseau-Nepton I, Kaduri S, Garfield N, Krishnamoorthy P.
J Pediatr Endocrinol Metab. 2014;27(1-2):117-21.
Hypothalamic hamartoma associated with central precocious puberty and growth hormone deficiency.
23314738
MALE Infant
Giant hypothalamic hamartoma: case report and literature review.
Alves C, Barbosa V, Machado M.
Childs Nerv Syst. 2013;29(3):513-6.
We present a 14-month-old boy with central precocious puberty and gelastic seizures in whom a magnetic resonance imaging scan revealed a giant hypothalamic hamartoma measuring 5082018201508201820140mm.
23746126
FEMALE Infant
Surgical treatment of hypothalamic hamartoma causing central precocious puberty: long-term follow-up.
Li CD, Luo SQ, Gong J, Ma ZY, Jia G, Zhang YQ, Li JF.
J Neurosurg Pediatr. 2013;12(2):151-4.
Surgical treatment of hypothalamic hamartoma causing central precocious puberty: long-term follow-up.
23746126
FEMALE Infant
Surgical treatment of hypothalamic hamartoma causing central precocious puberty: long-term follow-up.
Li CD, Luo SQ, Gong J, Ma ZY, Jia G, Zhang YQ, Li JF.
J Neurosurg Pediatr. 2013;12(2):151-4.
Hypothalamic hamartoma (HH) is a rare condition that often manifests as central precocious puberty (CPP).
22837930
(3401770)
OTHER
Central precocious puberty due to hypothalamic hamartoma in a six-month-old infant girl.
Kotwal N, Yanamandra U, Menon AS, Nair V.
Indian J Endocrinol Metab. 2012;16(4):627-30.
We present to you a case of isosexual (central), precocious puberty in a 16-month-old girl, who was symptomatic since the age of six months, and was later, diagnosed to have hypothalamic hamartoma.
22837930
(3401770)
OTHER
Central precocious puberty due to hypothalamic hamartoma in a six-month-old infant girl.
Kotwal N, Yanamandra U, Menon AS, Nair V.
Indian J Endocrinol Metab. 2012;16(4):627-30.
Central precocious puberty due to hypothalamic hamartoma in a six-month-old infant girl.
22145483
FEMALE Infant
Unique concurrent appearance of two rare conditions in a young girl: central precocious puberty due to hypothalamic hamartoma and uncommon type of diabetes.
Kocova M, Zdraveska N, Sukarova-Angelovska E.
J Pediatr Endocrinol Metab. 2011;24(9-10):815-8.
We present a girl with early onset of central precocious puberty at the age of 8 months, due to hypothalamic hamartoma.
21870566
FEMALE Infant
[Central precocious puberty due to hypothalamic hamartoma in Cameroon].
Mbassi Awa HD, Abena Obama MT, Pondy A, Pienkowski C, Nko'o Amvene S, Mbede J.
Med Trop (Mars). 2011;71(3):309-11.
Hypothalamic hamartoma must always be suspected in case of central precocious puberty.
19789152
MIXED_SAMPLE Infant
A rare case of central precocious puberty due to hypothalamic hamartoma diagnosed in utero.
Acharya SV, Gopal RA, Menon PS, Bandgar TR, Shah NS.
Endocr Pract. 2010;16(2):237-40.
To report a rare case of central precocious puberty attributable to hypothalamic hamartoma that was diagnosed in utero.
19789152
MIXED_SAMPLE Infant
A rare case of central precocious puberty due to hypothalamic hamartoma diagnosed in utero.
Acharya SV, Gopal RA, Menon PS, Bandgar TR, Shah NS.
Endocr Pract. 2010;16(2):237-40.
We present the clinical, laboratory, and imaging data pertaining to our case and discuss the diagnostic features and recommended treatment of central precocious puberty in patients with hypothalamic hamartoma.
19789152
MIXED_SAMPLE Infant
A rare case of central precocious puberty due to hypothalamic hamartoma diagnosed in utero.
Acharya SV, Gopal RA, Menon PS, Bandgar TR, Shah NS.
Endocr Pract. 2010;16(2):237-40.
On investigation, the patient was diagnosed as having hypothalamic hamartoma with central precocious puberty.
17541635
FEMALE Infant
Central precocious puberty due to hypothalamic hamartoma in a 7-month-old infant girl.
Rousso IH, Kourti M, Papandreou D, Tragiannidis A, Athanasiadou F.
Eur J Pediatr. 2008;167(5):583-5.
Central precocious puberty due to hypothalamic hamartoma in a 7-month-old infant girl.
17544949
MALE Child
Cognitive and behavioral dysfunction in children with hypothalamic hamartoma and epilepsy.
Prigatano GP.
Semin Pediatr Neurol. 2007;14(2):65-72.
Hypothalamic hamartoma (HH) syndrome comprises the clinical triad of epilepsy, developmental retardation, and central precocious puberty.
10190476
FEMALE Infant, Newborn
Oral-facial-digital syndrome with hypothalamic hamartoma, postaxial ray hypoplasia of the limbs, and vagino-cystic communication: a new variant?
Fujiwara I, Kondo Y, Iinuma K.
Am J Med Genet. 1999;83(2):77-81.
We report on a 20-month-old girl with hypothalamic hamartoma, left cerebral atrophy, tongue nodules, oral frenula, micrognathia, hypoplasia of the left ulna, the fibulae, and right tibia, polysyndactyly of the hands and feet, vagino-cystic drainage with hydrometrocolpos, megaloureters, and hydronephrosis, agenesis of urethra, complex partial seizures, and central precocious puberty.
8808013
FEMALE Infant
Precocious puberty and decreased melatonin secretion due to a hypothalamic hamartoma.
Commentz JC, Helmke K.
Horm Res. 1995;44(6):271-5.
We report for the first time the melatonin plasma values of a girl with central precocious puberty and gelastic seizures due to a hypothalamic hamartoma.
2533141
MIXED_SAMPLE Infant
Lack of adrenarche in two children with precocious puberty secondary to hypothalamic hamartoma.
Rappaport R, Brauner R.
Horm Res. 1989;31(5-6):226-9.
This report concerns 2 children with central precocious puberty secondary to hypothalamic hamartoma.